Chimeric antigen receptor cells for treating solid tumor

ABSTRACT

The compositions and methods described herein are directed to treating solid tumor using CAR T therapy. The compositions include CAR comprising an extracellular domain that binds a siglec protein or a receptor that binds the peptide hormone kisspeptin.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Patent Application 62/725,025, filed on Aug. 30, 2018; U.S. Provisional Patent Application 62/731,079, filed on Sep. 13, 2018; U.S. Provisional Patent Application 62/754,175, filed on Nov. 1, 2018; U.S. Provisional Patent Application 62/807,482, filed on Feb. 19, 2019; U.S. Provisional Patent Application 62/842,936, filed on May 3, 2019; and U.S. Provisional Patent Application 62/848,984, filed on May 16, 2019; which are hereby incorporated by reference in their entirety.

SEQUENCE LISTING INFORMATION

A computer readable textfile, entitled “SDS1.0053PCT 8-29-2019_ST25.txt,” created on or about Aug. 29, 2019 with a file size of about 533 KB, contains the sequence listing for this application and is hereby incorporated by reference in its entirety.

TECHNICAL FIELD

The present disclosure relates to modified cells and uses, in particular to compositions and methods for treating cancer using Chimeric Antigen Receptor (CAR) cells.

BACKGROUND

Most existing cancer treatment programs include surgery, radiotherapy, and chemotherapy, targeted therapy and immunotherapy. The drawbacks of the existing programs include poor treatment of advanced patients, side effects, patients with poor quality of life. For example, treatment of renal cancer includes resection, targeted therapy (anti-VEGF and mTOR inhibitor, etc.) and immunotherapy (IL-2, PD1 antibody, etc.). Treatment of pancreatic cancer includes surgical resection, radiotherapy, and chemotherapy. Treatment of urothelial carcinoma includes surgical resection, chemoradiation, targeted therapy, and immunotherapy. Treatment of breast cancer includes surgical resection, chemoradiation, targeted therapy, and immunotherapy. Treatment of ovarian cancer includes surgical resection, radiotherapy, chemotherapy, and targeted therapy. Treatment of prostate cancer includes surgical resection, chemoradiation, targeted therapy, and Immunotherapy. Treatment of esophageal cancer includes surgical resection, radiotherapy, and chemotherapy. Treatment of colorectal cancer includes surgical resection, radiotherapy, chemotherapy, and targeted therapy. Treatment of endometrial cancer: surgical resection, radiotherapy, chemotherapy, and targeted therapy.

SUMMARY

Embodiments relate to a discovery that some antigen have relatively low expression on tumor cells, as compared to the expression on normal tissues. Further, while expressed in normal tissues, some other antigens are specifically expressed in a certain tissue (e.g., a group of cells or an organ), and the killing of normal cells of the tissue does not cause a life-threatening event (e.g., complications) to the subject. Examples of the nonessential tissues include organs such as prostate, breast, or melanocyte. Accordingly, the embodiments of the present disclosure relate to a chimeric antigen receptor (CAR) including an extracellular domain that binds at least one of these antigens and treating the cancer using cells including the CAR.

Embodiments relate to compositions and methods for treating cancer using CAR cells. Embodiments relate to an isolated nucleic acid sequence encoding a CAR, wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, wherein the extracellular domain of the CAR binds an antigen of a solid tumor. The antigen may comprise SIGLEC15, SLC6A3, KISS1R, QRFPR, GPR119, CLDN6, UPK2, ADAM12, SLC45A3, ACPP, MUC21, MUC16, MS4A12, ALPP, SLC2A14, GS1-259H13.2, ERVFRD-1, ADGRG2, ECEL1, CHRNA2, GP2, or PSG9.

This Summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter.

BRIEF DESCRIPTION OF THE DRAWINGS

The Detailed Description is described with reference to the accompanying figures. The use of the same reference numbers in different figures indicates similar or identical items.

FIG. 1 shows a schematic diagram illustrating an example of a CAR structure.

FIG. 2 shows flow cytometry analysis of T cells expressing CARs.

FIG. 3 shows results of a killing assay of anti-SIGLEC15 CAR.

FIGS. 4 and 5 show results of cytokine release assays of anti-SIGLEC15 CAR.

FIG. 6 shows results of a killing assay of KISSR CAR.

FIG. 7 show results of a cytokine release assay of anti-KISSR CAR.

FIGS. 8, 9, and 10 show flow cytometry assay for ACPP antibodies.

FIG. 11 shows immunofluorescence staining of paraffin sections of prostate cancer.

FIG. 12 shows 293T cells expressing ACPP.

FIG. 13 shows cytometry assay of T cells expressing ACPP CAR.

FIG. 14 shows results of co-culturing assay.

FIG. 15 shows IFN-γ release of anti-ACPP CAR T cells in response to ACPP.

FIG. 16 shows that CAR expression of anti-ACPP CAR on T cells can be measured by detecting human CAR antibody.

FIG. 17 shows cytokine release assay of anti-ACPP CAR T cells.

FIGS. 18 and 19 show CD137 expression in various conditions.

FIG. 20 shows antibody titer against UPK2-His in mouse serum after ELISA assay.

FIG. 21 shows analysis of binding of 8 phage display antibodies to UPK2-His based on Phage-ELISA.

FIG. 22 shows ELISA analysis of the binding of recombinant monoclonal antibodies to recombinant UPK2-His.

FIG. 23 shows ELISA analysis of the specificity of recombinant anti-UPK2 mAb.

FIG. 24 shows an exemplary structure of a binding molecule.

FIG. 25 shows a table of markers and the uses thereof.

FIG. 26 shows an exemplary structure of a CAR.

DETAILED DESCRIPTION

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art to which the disclosure belongs. Although any method and material similar or equivalent to those described herein can be used in the practice or testing of the present disclosure, preferred methods and materials are described. For the purposes of the present disclosure, the following terms are defined below.

The articles “a” and “an” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.

By “about” is meant a quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length that varies by as much as 20, 15, 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1% to a reference quantity, level, value, number, frequency, percentage, dimension, size, amount, weight or length.

The term “activation,” as used herein, refers to the state of a cell that has been sufficiently stimulated to induce detectable cellular proliferation. Activation can also be associated with induced cytokine production and detectable effector functions. The term “activated T cells” refers to, among other things, T cells that are undergoing cell division.

The term “antibody” is used in the broadest sense and refers to monoclonal antibodies (including full length monoclonal antibodies), polyclonal antibodies, multi-specific antibodies (e.g., bispecific antibodies), and antibody fragments so long as they exhibit the desired biological activity or function. The antibodies in the present disclosure may exist in a variety of forms including, for example, polyclonal antibodies, monoclonal antibodies, Fv, Fab and F(ab)₂, as well as single chain antibodies and humanized antibodies (Harlow et al., 1999, In: Using Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, NY; Harlow et al., 1989, In: Antibodies: A Laboratory Manual, Cold Spring Harbor, N.Y.; Houston et al., 1988, Proc. Natl. Acad. Sci. USA 85:5879-5883; Bird et al., 1988, Science 242:423-426).

The term “antibody fragments” refers to a portion of a full length antibody, for example, the antigen binding or variable region of the antibody. Other examples of antibody fragments include Fab, Fab′, F(ab′)2, and Fv fragments; diabodies; linear antibodies; single-chain antibody molecules; and multi-specific antibodies formed from antibody fragments.

The term “Fv” refers to the minimum antibody fragment which contains a complete antigen-recognition and -binding site. This fragment consists of a dimer of one heavy- and one light-chain variable region domain in tight, non-covalent association. From the folding of these two domains emanates six hypervariable loops (3 loops each from the H and L chain) that contribute the amino acid residues for antigen binding and confer antigen binding specificity to the antibody. However, even a single variable domain (or half of a Fv including only three complementarity determining regions (CDRs) specific for an antigen) has the ability to recognize and bind antigen, although at a lower affinity than the entire binding site (the dimer).

An “antibody heavy chain,” as used herein, refers to the larger of the two types of polypeptide chains present in all antibody molecules in their naturally occurring conformations. An “antibody light chain,” as used herein, refers to the smaller of the two types of polypeptide chains present in all antibody molecules in their naturally occurring conformations. K and A light chains refer to the two major antibody light chain isotypes.

The term “synthetic antibody” refers to an antibody which is generated using recombinant DNA technology, such as, for example, an antibody expressed by a bacteriophage. The term also includes an antibody which has been generated by the synthesis of a DNA molecule encoding the antibody and the expression of the DNA molecule to obtain the antibody, or to obtain an amino acid encoding the antibody. The synthetic DNA is obtained using technology that is available and well known in the art.

The term “antigen” refers to a molecule that provokes an immune response, which may involve either antibody production, or the activation of specific immunologically-competent cells, or both. Antigens include any macromolecule, including all proteins or peptides, or molecules derived from recombinant or genomic DNA. For example, DNA including a nucleotide sequence or a partial nucleotide sequence encoding a protein or peptide that elicits an immune response, and therefore, encodes an “antigen” as the term is used herein. An antigen need not be encoded solely by a full-length nucleotide sequence of a gene. An antigen can be generated, synthesized or derived from a biological sample including a tissue sample, a tumor sample, a cell, or a biological fluid.

The term “anti-tumor effect” as used herein, refers to a biological effect associated with a decrease in tumor volume, a decrease in the number of tumor cells, a decrease in the number of metastases, decrease in tumor cell proliferation, decrease in tumor cell survival, an increase in life expectancy of a subject having tumor cells, or amelioration of various physiological symptoms associated with the cancerous condition. An “anti-tumor effect” can also be manifested by the ability of the peptides, polynucleotides, cells, and antibodies in the prevention of the occurrence of tumor in the first place.

The term “auto-antigen” refers to an antigen mistakenly recognized by the immune system as being foreign. Auto-antigens include cellular proteins, phosphoproteins, cellular surface proteins, cellular lipids, nucleic acids, glycoproteins, including cell surface receptors.

The term “autologous” is used to describe a material derived from a subject which is subsequently re-introduced into the same subject.

The term “allogeneic” is used to describe a graft derived from a different subject of the same species. As an example, a donor subject may be a related or unrelated or recipient subject, but the donor subject has immune system markers which are similar to the recipient subject.

The term “xenogeneic” is used to describe a graft derived from a subject of a different species. As an example, the donor subject is from a different species than a recipient subject and the donor subject and the recipient subject can be genetically and immunologically incompatible.

The term “cancer” refers to a disease characterized by the rapid and uncontrolled growth of aberrant cells. Cancer cells can spread locally or through the bloodstream and lymphatic system to other parts of the body. Examples of various cancers include breast cancer, prostate cancer, ovarian cancer, cervical cancer, skin cancer, pancreatic cancer, colorectal cancer, renal cancer, liver cancer, brain cancer, lymphoma, leukemia, lung cancer, and the like.

Cancers that may be treated include tumors that are not vascularized, or not yet substantially vascularized, as well as vascularized tumors. The cancers may include non-solid tumors (such as hematological tumors, for example, leukemias and lymphomas) or may include solid tumors. Types of cancers to be treated with the CARs of the disclosure include, but are not limited to, carcinoma, blastoma, and sarcoma, and certain leukemia or lymphoid malignancies, benign and malignant tumors, and malignancies, e.g., sarcomas, carcinomas, and melanomas. Adult tumors/cancers and pediatric tumors/cancers are also included.

Hematologic cancers are cancers of the blood or bone marrow. Examples of hematological (or hematogenous) cancers include leukemias, including acute leukemias (such as acute lymphocytic leukemia, acute myelocytic leukemia, acute myelogenous leukemia and myeloblastic, promyelocytic, myelomonocytic, monocytic and erythroleukemia), chronic leukemias (such as chronic myelocytic (granulocytic) leukemia, chronic myelogenous leukemia, and chronic lymphocytic leukemia), polycythemia vera, lymphoma, Hodgkin's disease, non-Hodgkin's lymphoma (indolent and high grade forms), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, myelodysplastic syndrome, hairy cell leukemia and myelodysplasia.

Solid tumors are abnormal masses of tissue that usually do not contain cysts or liquid areas. Solid tumors can be benign or malignant. Different types of solid tumors are named for the type of cells that form them (such as sarcomas, carcinomas, and lymphomas). Examples of solid tumors, such as sarcomas and carcinomas, include fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, lymphoid malignancy, pancreatic cancer, breast cancer, lung cancers, ovarian cancer, prostate cancer, hepatocellular carcinoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, medullary thyroid carcinoma, papillary thyroid carcinoma, pheochromocytomas sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, Wilms' tumor, cervical cancer, testicular tumor, seminoma, bladder carcinoma, melanoma, and CNS tumors (such as a glioma (such as brainstem glioma and mixed gliomas), glioblastoma (also known as glioblastoma multiforme), astrocytoma, CNS lymphoma, germinoma, medulloblastoma, Schwannoma craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, neuroblastoma, retinoblastoma, and brain metastases).

A solid tumor antigen is an antigen expressed on a solid tumor. In embodiments, solid tumor antigens are also expressed at low levels on healthy tissue. Examples of solid tumor antigens and their related disease tumors are provided in Table 1.

TABLE 1 Solid Tumor antigen Disease tumor PRLR Breast Cancer CLCA1 colorectal Cancer MUC12 colorectal Cancer GUCY2C colorectal Cancer GPR35 colorectal Cancer CR1L Gastric Cancer MUC 17 Gastric Cancer TMPRSS11B esophageal Cancer MUC21 esophageal Cancer TMPRSS11E esophageal Cancer CD207 bladder Cancer SLC30A8 pancreatic Cancer CFC1 pancreatic Cancer SLC12A3 Cervical Cancer SSTR1 Cervical tumor GPR27 Ovary tumor FZD10 Ovary tumor TSHR Thyroid Tumor SIGLEC15 Urothelial cancer SLC6A3 Renal cancer KISS1R Renal cancer QRFPR Renal cancer: GPR119 Pancreatic cancer CLDN6 Endometrial cancer Urothelial cancer UPK2 Urothelial cancer (including bladder cancer) ADAM12 Breast cancer, pancreatic cancer and the like SLC45A3 Prostate cancer ACPP Prostate cancer MUC21 Esophageal cancer MUC16 Ovarian cancer MS4A12 Colorectal cancer ALPP Endometrial cancer CEA Colorectal carcinoma EphA2 Glioma FAP Mesothelioma GPC3 Lung squamous cell carcinoma IL13-Rα2 Glioma Mesothelin Metastatic cancer PSMA Prostate cancer ROR1 Breast lung carcinoma VEGFR-II Metastatic cancer GD2 Neuroblastoma FR-α Ovarian carcinoma ErbB2 Carcinomas EpCAM Carcinomas EGFRvIII Glioma-Glioblastoma EGFR Glioma-NSCL cancer tMUC 1 Cholangiocarcinoma, Pancreatic cancer, Breast PSCA pancreas, stomach, or prostate cancer

Throughout this specification, unless the context requires otherwise, the words “comprise,” “includes” and “including” will be understood to imply the inclusion of a stated step or element (ingredients or components) or group of steps or elements (ingredients or components) but not the exclusion of any other step or element or group of steps or elements.

The phrase “consisting of” is meant to include, and is limited to, whatever follows the phrase “consisting of.” Thus, the phrase “consisting of” indicates that the listed elements are required or mandatory and that no other elements may be present.

The phrase “consisting essentially of” is meant to include any element listed after the phrase and can include other elements that do not interfere with or contribute to the activity or action specified in the disclosure for the listed elements. Thus, the phrase “consisting essentially of” indicates that the listed elements are required or mandatory, but that other elements are optional and may or may not be present depending upon whether or not they affect the activity or action of the listed elements.

The terms “complementary” and “complementarity” refer to polynucleotides (i.e., a sequence of nucleotides) related by the base-pairing rules. For example, the sequence “A-G-T,” is complementary to the sequence “T-C-A.” Complementarity may be “partial,” in which only some of the nucleic acids' bases are matched according to the base pairing rules or there may be “complete” or “total” complementarity between the nucleic acids. The degree of complementarity between nucleic acid strands has significant effects on the efficiency and strength of hybridization between nucleic acid strands.

The term “corresponds to” or “corresponding to” refers to (a) a polynucleotide having a nucleotide sequence that is substantially identical or complementary to all or a portion of a reference polynucleotide sequence or encoding an amino acid sequence identical to an amino acid sequence in a peptide or protein; or (b) a peptide or polypeptide having an amino acid sequence that is substantially identical to a sequence of amino acids in a reference peptide or protein.

The term “costimulatory ligand” refers to a molecule on an antigen presenting cell (e.g., an APC, dendritic cell, B cell, and the like) that specifically binds a cognate costimulatory molecule on a T cell, thereby providing a signal which, in addition to the primary signal provided by, for instance, binding of a TCR/CD3 complex with an MHC molecule loaded with peptide, mediates a T cell response, including at least one of proliferation, activation, differentiation, and other cellular responses. A costimulatory ligand can include B7-1 (CD80), B7-2 (CD86), PD-L1, PD-L2, 4-1 BBL, OX40L, inducible co-stimulatory ligand (ICOS-L), intercellular adhesion molecule (ICAM), CD30L, CD40, CD70, CD83, HLA-G, MICA, MICB, HVEM, lymphotoxin beta receptor, 3/TR6, ILT3, ILT4, HVEM, a ligand for CD7, an agonist or antibody that binds the Toll ligand receptor and a ligand that specifically binds with B7-H3. A co-stimulatory ligand also includes, inter alia, an agonist or an antibody that specifically binds with a co-stimulatory molecule present on a T cell, such as CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and a ligand that specifically binds CD83.

The term “co-stimulatory molecule” refers to the cognate binding partner on a T cell that specifically binds with a co-stimulatory ligand, thereby mediating a co-stimulatory response by the T cell, such as proliferation. Co-stimulatory molecules include an MHC class I molecule, BTLA, and a Toll-like receptor.

The term “co-stimulatory signal” refers to a signal, which in combination with a primary signal, such as TCR/CD3 ligation, leads to T cell proliferation and/or upregulation or downregulation of key molecules. The terms “disease” and “condition” may be used interchangeably or may be different in that the particular malady or condition may not have a known causative agent (so that etiology has not yet been worked out), and it is therefore not yet recognized as a disease but only as an undesirable condition or syndrome, wherein a more or less specific set of symptoms have been identified by clinicians. The term “disease” is a state of health of a subject wherein the subject cannot maintain homeostasis, and wherein if the disease is not ameliorated then the subject's health continues to deteriorate. In contrast, a “disorder” in a subject is a state of health in which the animal is able to maintain homeostasis, but in which the animal's state of health is less favorable than it would be in the absence of the disorder. Left untreated, a disorder does not necessarily cause a further decrease in the animal's state of health.

The term “effective” refers to adequate to accomplish a desired, expected, or intended result. For example, an “effective amount” in the context of treatment may be an amount of a compound sufficient to produce a therapeutic or prophylactic benefit.

The term “encoding” refers to the inherent property of specific sequences of nucleotides in a polynucleotide, such as a gene, a cDNA, or an mRNA, to serve as templates for synthesis of other polymers and macromolecules in biological processes having either a defined sequence of nucleotides (i.e., rRNA, tRNA and mRNA) or a defined sequence of amino acids and the biological properties resulting therefrom. Thus, a gene encodes a protein if transcription and translation of mRNA corresponding to that gene produces the protein in a cell or other biological system. Both the coding strand, the nucleotide sequence of which is identical to the mRNA sequence (except that a “T” is replaced by a “U”) and is usually provided in sequence listings, and the non-coding strand, used as the template for transcription of a gene or cDNA, can be referred to as encoding the protein or other product of that gene or cDNA.

The term “exogenous” refers to a molecule that does not naturally occur in a wild-type cell or organism but is typically introduced into the cell by molecular biological techniques. Examples of exogenous polynucleotides include vectors, plasmids, and/or man-made nucleic acid constructs encoding the desired protein. With regard to polynucleotides and proteins, the term “endogenous” or “native” refers to naturally-occurring polynucleotide or amino acid sequences that may be found in a given wild-type cell or organism. Also, a particular polynucleotide sequence that is isolated from a first organism and transferred to a second organism by molecular biological techniques is typically considered an “exogenous” polynucleotide or amino acid sequence with respect to the second organism. In specific embodiments, polynucleotide sequences can be “introduced” by molecular biological techniques into a microorganism that already contains such a polynucleotide sequence, for instance, to create one or more additional copies of an otherwise naturally-occurring polynucleotide sequence, and thereby facilitate overexpression of the encoded polypeptide.

The term “expression” refers to the transcription and/or translation of a particular nucleotide sequence driven by its promoter.

The term “expression vector” refers to a vector including a recombinant polynucleotide including expression control sequences operably linked to a nucleotide sequence to be expressed. An expression vector includes sufficient cis-acting elements for expression; other elements for expression can be supplied by the host cell or in an in vitro expression system. Expression vectors include all those known in the art, such as cosmids, plasmids (e.g., naked or contained in liposomes) and viruses (e.g., lentiviruses, retroviruses, adenoviruses, and adeno-associated viruses) that incorporate the recombinant polynucleotide.

The term “homologous” refers to sequence similarity or sequence identity between two polypeptides or between two polynucleotides when a position in both of the two compared sequences is occupied by the same base or amino acid monomer subunit, e.g., if a position in each of two DNA molecules is occupied by adenine, then the molecules are homologous at that position. The percent of homology between two sequences is a function of the number of matching or homologous positions shared by the two sequences divided by the number of positions compared ×100. For example, if 6 of 10 of the positions in two sequences are matched or homologous then the two sequences are 60% homologous. By way of example, the DNA sequences ATTGCC and TATGGC share 50% homology. A comparison is made when two sequences are aligned to give maximum homology.

The term “immunoglobulin” or “Ig,” refers to a class of proteins, which function as antibodies. The five members included in this class of proteins are IgA, IgG, IgM, IgD, and IgE. IgA is the primary antibody that is present in body secretions, such as saliva, tears, breast milk, gastrointestinal secretions and mucus secretions of the respiratory and genitourinary tracts. IgG is the most common circulating antibody. IgM is the main immunoglobulin produced in the primary immune response in most subjects. It is the most efficient immunoglobulin in agglutination, complement fixation, and other antibody responses, and is important in defense against bacteria and viruses. IgD is the immunoglobulin that has no known antibody function but may serve as an antigen receptor. IgE is the immunoglobulin that mediates immediate hypersensitivity by causing the release of mediators from mast cells and basophils upon exposure to the allergen.

The term “isolated” refers to a material that is substantially or essentially free from components that normally accompany it in its native state. The material can be a cell or a macromolecule such as a protein or nucleic acid. For example, an “isolated polynucleotide,” as used herein, refers to a polynucleotide, which has been purified from the sequences which flank it in a naturally-occurring state, e.g., a DNA fragment which has been removed from the sequences that are normally adjacent to the fragment. Alternatively, an “isolated peptide” or an “isolated polypeptide” and the like, as used herein, refer to in vitro isolation and/or purification of a peptide or polypeptide molecule from its natural cellular environment, and from association with other components of the cell.

The term “substantially purified” refers to a material that is substantially frr from components that normally associated with it in its native state. For example, a substantially purified cell refers to a cell that has been separated from other cell types with which it is normally associated in its naturally occurring or native state. In some instances, a population of substantially purified cells refers to a homogenous population of cells. In other instances, this term refers simply to a cell that has been separated from the cells with which they are naturally associated in their natural state. In embodiments, the cells are cultured in vitro. In embodiments, the cells are not cultured in vitro.

In the context of the present disclosure, the following abbreviations for the commonly occurring nucleic acid bases are used. “A” refers to adenosine, “C” refers to cytosine, “G” refers to guanosine, “T” refers to thymidine, and “U” refers to uridine.

Unless otherwise specified, a “nucleotide sequence encoding an amino acid sequence” includes all nucleotide sequences that are degenerate versions of each other and that encode the same amino acid sequence. The phrase nucleotide sequence that encodes a protein or an RNA may also include introns to the extent that the nucleotide sequence encoding the protein may in some version contain an intron(s).

The term “lentivirus” refers to a genus of the Retroviridae family. Lentiviruses are unique among the retroviruses in being able to infect non-dividing cells; they can deliver a significant amount of genetic information into the DNA of the host cell, so they are one of the most efficient methods of a gene delivery vector. Moreover, the use of lentiviruses enables integration of the genetic information into the host chromosome resulting in stably transduced genetic information. HIV, SIV, and FIV are all examples of lentiviruses. Vectors derived from lentiviruses offer the means to achieve significant levels of gene transfer in vivo.

The term “modulating,” refers to mediating a detectable increase or decrease in the level of a response in a subject compared with the level of a response in the subject in the absence of a treatment or compound, and/or compared with the level of a response in an otherwise identical but untreated subject. The term encompasses perturbing and/or affecting a native signal or response thereby mediating a beneficial therapeutic response in a subject, preferably, a human.

Nucleic acid is “operably linked” when it is placed into a functional relationship with another nucleic acid sequence. For example, DNA for a presequence or secretory leader is operably linked to DNA for a polypeptide if it is expressed as a preprotein that participates in the secretion of the polypeptide; a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation.

The term “under transcriptional control” refers to a promoter being operably linked to and in the correct location and orientation in relation to a polynucleotide to control the initiation of transcription by RNA polymerase and expression of the polynucleotide.

The term “overexpressed” tumor antigen or “overexpression” of the tumor antigen is intended to indicate an abnormal level of expression of the tumor antigen in a cell from a disease area such as a solid tumor within a specific tissue or organ of the patient relative to the level of expression in a normal cell from that tissue or organ. Patients having solid tumors or a hematological malignancy characterized by overexpression of the tumor antigen can be determined by standard assays known in the art.

The term “parenteral administration” of a composition includes, e.g., subcutaneous (s.c.), intravenous (i.v.), intramuscular (i.m.), intrasternal injection, or infusion techniques.

The terms “patient,” “subject,” and “individual,” and the like are used interchangeably herein, and refer to any human, animal, or living organism, amenable to the methods described herein. In certain non-limiting embodiments, the patient, subject, or individual is a human or animal. In embodiments, the term “subject” is intended to include living organisms in which an immune response can be elicited (e.g., mammals). Examples of subjects include humans, and animals such as dogs, cats, mice, rats, and transgenic species thereof.

A subject in need of treatment or in need thereof includes a subject having a disease, condition, or disorder that needs to be treated. A subject in need thereof also includes a subject that needs treatment for prevention of a disease, condition, or disorder. In embodiments, the disease is cancer.

The term “polynucleotide” or “nucleic acid” refers to mRNA, RNA, cRNA, rRNA, cDNA or DNA. The term typically refers to a polymeric form of nucleotides of at least 10 bases in length, either ribonucleotides or deoxynucleotides or a modified form of either type of nucleotide. The term includes all forms of nucleic acids including single and double stranded forms of nucleic acids.

The terms “polynucleotide variant” and “variant” and the like refer to polynucleotides displaying substantial sequence identity with a reference polynucleotide sequence or polynucleotides that hybridize with a reference sequence under stringent conditions that are defined hereinafter. These terms also encompass polynucleotides that are distinguished from a reference polynucleotide by the addition, deletion or substitution of at least one nucleotide. Accordingly, the terms “polynucleotide variant” and “variant” include polynucleotides in which one or more nucleotides have been added or deleted or replaced with different nucleotides. In this regard, it is well understood in the art that certain alterations inclusive of mutations, additions, deletions, and substitutions can be made to a reference polynucleotide whereby the altered polynucleotide retains the biological function or activity of the reference polynucleotide or has increased activity in relation to the reference polynucleotide (i.e., optimized). Polynucleotide variants include, for example, polynucleotides having at least 50% (and at least 51% to at least 99% and all integer percentages in between, e.g., 90%, 95%, or 98%) sequence identity with a reference polynucleotide sequence described herein. The terms “polynucleotide variant” and “variant” also include naturally-occurring allelic variants and orthologs.

The terms “polypeptide,” “polypeptide fragment,” “peptide,” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues and to variants and synthetic analogues of the same. Thus, these terms apply to amino acid polymers in which one or more amino acid residues are synthetic non-naturally occurring amino acids, such as a chemical analogue of a corresponding naturally occurring amino acid, as well as to naturally-occurring amino acid polymers. In certain aspects, polypeptides may include enzymatic polypeptides, or “enzymes,” which typically catalyze (i.e., increase the rate of) various chemical reactions.

The term “polypeptide variant” refers to polypeptides that are distinguished from a reference polypeptide sequence by the addition, deletion, or substitution of at least one amino acid residue. In embodiments, a polypeptide variant is distinguished from a reference polypeptide by one or more substitutions, which may be conservative or non-conservative. In embodiments, the polypeptide variant comprises conservative substitutions and, in this regard, it is well understood in the art that some amino acids may be changed to others with broadly similar properties without changing the nature of the activity of the polypeptide. Polypeptide variants also encompass polypeptides in which one or more amino acids have been added or deleted or replaced with different amino acid residues.

The term “promoter” refers to a DNA sequence recognized by the synthetic machinery of the cell or introduced synthetic machinery, required to initiate the specific transcription of a polynucleotide sequence. The term “expression control sequences” refers to DNA sequences necessary for the expression of an operably linked coding sequence in a particular host organism. The control sequences that are suitable for prokaryotes, for example, include a promoter, optionally an operator sequence, and a ribosome binding site. Eukaryotic cells are known to utilize promoters, polyadenylation signals, and enhancers.

The term “bind,” “binds,” or “interacts with” refers to a molecule recognizing and adhering to a second molecule in a sample or organism but does not substantially recognize or adhere to other structurally unrelated molecules in the sample. The term “specifically binds,” as used herein with respect to an antibody, refers to an antibody which recognizes a specific antigen, but does not substantially recognize or bind other molecules in a sample. For example, an antibody that specifically binds an antigen from one species may also bind that antigen from one or more species. But, such cross-species reactivity does not itself alter the classification of an antibody as specific. In another example, an antibody that specifically binds an antigen may also bind different allelic forms of the antigen. However, such cross reactivity does not itself alter the classification of an antibody as specific. In some instances, the terms “specific binding” or “specifically binding,” can be used in reference to the interaction of an antibody, a protein, or a peptide with a second chemical species, to mean that the interaction is dependent upon the presence of a particular structure (e.g., an antigenic determinant or epitope) on the chemical species; for example, an antibody recognizes and binds a specific protein structure rather than to any protein. If an antibody is specific for epitope “A,” the presence of a molecule containing epitope A (or free, unlabeled A), in a reaction containing labeled “A” and the antibody, will reduce the amount of labeled A bound to the antibody.

A “binding protein” is a protein that is able to bind non-covalently to another molecule. A binding protein can bind to, for example, a DNA molecule (a DNA-binding protein), an RNA molecule (an RNA-binding protein) and/or a protein molecule (a protein-binding protein). In the case of a protein-binding protein, it can bind to itself (to form homodimers, homotrimers, etc.) and/or it can bind to one or more molecules of a different protein or proteins. A binding protein can have more than one type of binding activity. For example, zinc finger proteins have DNA-binding, RNA-binding, and protein-binding activity.

A “zinc finger DNA binding protein” (or binding domain) is a protein, or a domain within a larger protein, that binds DNA in a sequence-specific manner through one or more zinc fingers, which are regions of amino acid sequence within the binding domain whose structure is stabilized through coordination of a zinc ion. The term zinc finger DNA binding protein is often abbreviated as zinc finger protein or ZFP.

Zinc finger binding domains can be “engineered” to bind to a predetermined nucleotide sequence, for example via engineering (altering one or more amino acids) of the recognition helix region of a naturally occurring zinc finger protein. Further, a Zinc finger binding domain may be fused a DNA-cleavage domain to form a Zinc finger nuclease (ZFN) targeting a specific desired DNA sequence. For example, a pair of ZFNs (e.g., a ZFN-left arm and a ZFN-right arm) may be engineered to target and cause modifications of specific desired DNA sequences (e.g., TRAC genes).

“Cleavage” refers to the breakage of the covalent backbone of a DNA molecule. Cleavage can be initiated by a variety of methods including, but not limited to, enzymatic or chemical hydrolysis of a phosphodiester bond. Both single-stranded cleavage and double-stranded cleavage are possible, and double-stranded cleavage can occur as a result of two distinct single-stranded cleavage events. DNA cleavage can result in the production of either blunt ends or staggered ends. In embodiments, fusion polypeptides are used for targeted double-stranded DNA cleavage.

A “target site” or “target sequence” is a nucleic acid sequence that defines a portion of a nucleic acid to which a binding molecule will bind, provided sufficient conditions for binding exist. For example, the sequence 5′ GAATTC 3′ is a target site for the Eco RI restriction endonuclease.

A “fusion” molecule is a molecule in which two or more subunit molecules are linked, preferably covalently. The subunit molecules can be the same chemical type of molecule or can be different chemical types of molecules. Examples of the first type of fusion molecule include, but are not limited to, fusion proteins (for example, a fusion between a ZFP DNA-binding domain and one or more activation domains) and fusion nucleic acids (for example, a nucleic acid encoding the fusion protein described supra). Examples of the second type of fusion molecule include, but are not limited to, a fusion between a triplex-forming nucleic acid and a polypeptide, and a fusion between a minor groove binder and a nucleic acid.

Expression of a fusion protein in a cell can result from delivery of the fusion protein to the cell or by delivery of a polynucleotide encoding the fusion protein to a cell, wherein the polynucleotide is transcribed, and the transcript is translated, to generate the fusion protein. Trans-splicing, polypeptide cleavage, and polypeptide ligation can also be involved in the expression of the protein in a cell. Methods for polynucleotide and polypeptide delivery to cells are presented elsewhere in this disclosure.

“Modulation” of gene expression refers to a change in the activity of a gene. Modulation of expression can include but is not limited to, gene activation and gene repression. Genome editing (e.g., cleavage, alteration, inactivation, random mutation) can be used to modulate expression. Gene inactivation refers to any reduction in gene expression as compared to a cell that does not include a ZFP as described herein. Thus, gene inactivation may be partial or complete.

A “region of interest” is any region of cellular chromatin, such as, for example, a gene or a non-coding sequence within or adjacent to a gene, in which it is desirable to bind an exogenous molecule. Binding can be for the purposes of targeted DNA cleavage and/or targeted recombination. A region of interest can be present in a chromosome, an episome, an organellar genome (e.g., mitochondrial, chloroplast), or an infecting viral genome, for example. A region of interest can be within the coding region of a gene, within transcribed non-coding regions such as, for example, leader sequences, trailer sequences or introns, or within non-transcribed regions, either upstream or downstream of the coding region. A region of interest can be as small as a single nucleotide pair or up to 2,000 nucleotide pairs in length, or any integral value of nucleotide pairs.

By “statistically significant,” it is meant that the result was unlikely to have occurred by chance. Statistical significance can be determined by any method known in the art. Commonly used measures of significance include the p-value, which is the frequency or probability with which the observed event would occur if the null hypothesis were true. If the obtained p-value is smaller than the significance level, then the null hypothesis is rejected. In simple cases, the significance level is defined at a p-value of 0.05 or less. A “decreased” or “reduced” or “lesser” amount is typically a “statistically significant” or a physiologically significant amount, and may include a decrease that is about 1.1, 1.2, 1.3, 1.4, 1.5, 1.6 1.7, 1.8, 1.9, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, or 50 or more times (e.g., 100, 500, 1000 times) (including all integers and decimal points in between and above 1, e.g., 1.5, 1.6, 1.7. 1.8, etc.) an amount or level described herein.

The term “stimulation,” refers to a primary response induced by binding of a stimulatory molecule (e.g., a TCR/CD3 complex) with its cognate ligand thereby mediating a signal transduction event, such as signal transduction via the TCR/CD3 complex. Stimulation can mediate altered expression of certain molecules, such as downregulation of TGF-β, and/or reorganization of cytoskeletal structures. CD3 zeta is not the only suitable primary signaling domain for a CAR construct with respect to the primary response. For example, back in 1993, both CD3 zeta and FcR gamma were shown as functional primary signaling domains of CAR molecules. Eshhar et al., “Specific activation and targeting of cytotoxic lymphocytes through chimeric single chains consisting of antibody-binding domains and the gamma or zeta subunits of the immunoglobulin and T cell receptors” PNAS, 1993 Jan. 15; 90(2):720-4, showed that two CAR constructs in which an scFv was fused to “either the FcR gamma chain or the CD3 complex chain” triggered T cell activation and target cell. Notably, as demonstrated in Eshhar et al., CAR constructs containing only the primary signaling domain CD3 zeta or FcR gamma are functional without the co-presence of co-stimulatory domains. Additional non-CD3 zeta based CAR constructs have been developed over the years. For example, Wang et al. (,“A Chimeric Antigen Receptor (CARs) Based Upon a Killer Immunoglobulin-Like Receptor (KIR) Triggers Robust Cytotoxic Activity in Solid Tumors” Molecular Therapy, vol. 22, no. Suppl.1, May 2014, page S57) tested a CAR molecule in which an scFv was fused to “the transmembrane and cytoplasmic domain of’ a killer immunoglobulin-like receptor (KIR). Wang et al. reported that, “a KIR-based CAR targeting mesothelin (SS 1-KIR) triggers antigen-specific cytotoxic activity and cytokine production that is comparable to CD3˜-based CARs.” A second publication from the same group, Wang et al. (“Generation of Potent T-cell Immunotherapy for Cancer Using DAP12-Based, Multichain, Chimeric Immunoreceptors” Cancer Immunol Res. 2015 July; 3(7):815-26) showed that a CAR molecule in which “a single-chain variable fragment for antigen recognition was fused to the transmembrane and cytoplasmic domains of KIR2DS2, a stimulatory killer immunoglobulin-like receptor (KIR)” functioned both in vitro and in vivo “when introduced into human T cells with DAP12, an immunotyrosine-based activation motifs-containing adaptor.”

The term “stimulatory molecule” refers to a molecule on a T cell that specifically binds a cognate stimulatory ligand present on an antigen presenting cell. For example, a functional signaling domain derived from a stimulatory molecule is the zeta chain associated with the T cell receptor complex.

The term “stimulatory ligand” refers to a ligand that when present on an antigen presenting cell (e.g., an APC, a dendritic cell, a B-cell, and the like.) can specifically bind with a cognate binding partner (referred to herein as a “stimulatory molecule”) on a cell, for example a T cell, thereby mediating a primary response by the T cell, including activation, initiation of an immune response, proliferation, and similar processes. Stimulatory ligands are well-known in the art and encompass, inter alia, an MHC Class I molecule loaded with a peptide, an anti-CD3 antibody, a superagonist anti-CD28 antibody, and a superagonist anti-CD2 antibody.

The term “therapeutic” refers to a treatment and/or prophylaxis. A therapeutic effect is obtained by suppression, remission, or eradication of a disease state or alleviating the symptoms of a disease state.

The term “therapeutically effective amount” refers to the amount of the subject compound that will elicit the biological or medical response of a tissue, system, or subject that is being sought by the researcher, veterinarian, medical doctor or another clinician. The term “therapeutically effective amount” includes that amount of a compound that, when administered, is sufficient to prevent the development of, or alleviate to some extent, one or more of the signs or symptoms of the disorder or disease being treated. The therapeutically effective amount will vary depending on the compound, the disease and its severity and the age, weight, etc., of the subject to be treated.

The term “treat a disease” refers to the reduction of the frequency or severity of at least one sign or symptom of a disease or disorder experienced by a subject.

The term “transfected” or “transformed” or “transduced” refers to a process by which an exogenous nucleic acid is transferred or introduced into the host cell. A “transfected” or “transformed” or “transduced” cell is one which has been transfected, transformed, or transduced with exogenous nucleic acid. The cell includes the primary subject cell and its progeny.

The term “vector” refers to a polynucleotide that comprises an isolated nucleic acid and which can be used to deliver the isolated nucleic acid to the interior of a cell in vitro and in vivo (in a subject). Numerous vectors are known in the art including linear polynucleotides, polynucleotides associated with ionic or amphiphilic compounds, plasmids, and viruses. Thus, the term “vector” includes an autonomously replicating plasmid or a virus. The term also includes non-plasmid and non-viral compounds which facilitate transfer of nucleic acid into cells, such as, for example, polylysine compounds, liposomes, and the like. Examples of viral vectors include, adenoviral vectors, adeno-associated virus vectors, retroviral vectors, and others. For example, lentiviruses are complex retroviruses, which, in addition to the common retroviral genes gag, pol, and env, contain other genes with regulatory or structural function. Lentiviral vectors are well known in the art. Some examples of lentivirus include the Human Immunodeficiency Viruses: HIV-1, HIV-2, and the Simian Immunodeficiency Virus: SIV. Lentiviral vectors have been generated by multiply attenuating the HIV virulence genes, for example, the genes env, vif, vpr, vpu, and nef are deleted making the vector biologically safe.

Ranges: throughout this disclosure, various aspects of the disclosure can be presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the disclosure. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 2.7, 3, 4, 5, 5.3, and 6. This applies regardless of the breadth of the range.

Embodiments of the present disclosure relate to treating cancer using chimeric antigen receptor (CAR) cells. Embodiments relate to an isolated nucleic acid encoding a CAR, wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, wherein the extracellular domain of the CAR binds an antigen of a solid tumor. For example, transcriptional data shows that expression of antigens such as SLC6A3, KISS1R, QRFPR in normal tissues is very low, but expression of such antigens in cells related to renal cancer is high. Information of some of the antigens is provided below in Table 2.

TABLE 2 Subcellular Organ mainly Target Target SEQ Gene name localization expressing Tumor ID NO. SIGLEC15 Plasma Expression Urothelial 17 membrane in all normal cancer tissues is very low SLC6A3 Plasma Expression Renal 18 membrane in all normal cancer tissues is very low KISS1R Plasma Expression Renal 19 membrane in all normal cancer tissues is very low QRFPR Plasma Expression Renal 20 membrane in all normal cancer: tissues is very low GPR119 Plasma Expression Pancreatic 21 membrane in all normal cancer tissues is very low CLDN6 Plasma Expression Endometrial 22 membrane in all normal cancer/ tissues is Urothelial very low cancer UPK2 Plasma Urethra/ Urothelial  1 membrane bladder cancer (including bladder cancer) ADAM12 Plasma placenta Breast cancer,  2 membrane pancreatic cancer and the like SLC45A3 Plasma prostate Prostate  3 membrane cancer ACPP Plasma prostate Prostate  4 membrane cancer MUC21 Plasma esophagus Esophageal  5 membrane cancer MUC16 Plasma Cervical/ Ovarian  6 membrane Fallopian tube cancer MS4A12 Plasma the large Colorectal  7 membrane intestine cancer ALPP Plasma Placenta/ Endometrial  8 membrane cervix cancer SLC2A14 Plasma testis Testicular  9 membrane cancer GS1- Plasma testis Thyroid 10 259H13.2 membrane cancer or glioma or testicular cancer and other ERVFRD-1 Plasma Placenta or Kidney 11 membrane parathyroid cancer or Urethral cancer and many others ADGRG2 Plasma Epididymis Ovarian 12 membrane cancer ECEL1 Plasma Ovary Endometrial 13 membrane cancer CHRNA2 Plasma Prostate or Prostate 14 membrane cortex cancer GP2 Plasma pancreas Pancreatic 15 membrane cancer PSG9 Plasma placenta Kidney 16 membrane cancer or liver cancer

In embodiments, the extracellular domain of the CAR binds SIGLEC15. SIGLEC15 is a receptor protein expressed on the cell membrane, which recognizes sialylated glycans. Transcriptional data predict that it is overexpressed in urothelial cancer cells and is expressed at a low level in normal tissues. It is mainly found in spleen and lymph nodes, and other immune organs have a certain amount of low expression. For example, the extracellular domain of the CAR binds SIGLEC15 having the amino acid sequence of SEQ ID NO: 17. In embodiments, the extracellular domain comprises one of the amino acid sequences of SEQ ID NOs: 45-56. Embodiments relate to a method of eliciting and/or enhancing T cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR to the subject. In embodiments, the tumor is associated with urothelial cancer.

The T cell response in a subject refers to cell-mediated immunity associated with a helper, killer, regulatory, and other types T cells. For example, T cell response may include activities such as assistance to other white blood cells in immunologic processes and identifying and destroying virus-infected cells and tumor cells. T cell response in the subject may be measured via various indicators such as a number of virus-infected cells and/or tumor cells that T cells kill, an amount of cytokines that T cells release in co-culturing with virus-infected cells and/or tumor cells, a level of proliferation of T cells in the subject, a phenotype change of T cells (e.g., changes to memory T cells), and a level longevity or lifetime of T cells in the subject.

In embodiments, in vitro killing assay may be performed by measuring the killing efficacy of CAR T cells by co-culturing CAR T cells with antigen-positive cells. CAR T cells may be considered to have killing effect on the corresponding antigen-positive cells by showing a decrease in the number of corresponding antigen-positive cells co-cultured with CAR T cells and an increase in the release of IFNγ, TNFα, etc. as compared to control cells that do not express the corresponding antigen. Further, in vivo antitumor activity of the CAR T cells may be tested. For example, xenograft models may be established using the antigens described herein in immunodeficient mice. Heterotransplantation of human cancer cells or tumor biopsies into immunodeficient rodents (xenograft models) has, for the past two decades, constituted the major preclinical screen for the development of novel cancer therapeutics (Song et al., Cancer Res. PMC 2014 Aug. 21, and Morton et al., Nature Protocols, 2, -247-250 (2007)). To evaluate the anti-tumor activity of CAR T cells in vivo, immunodeficient mice bearing tumor xenografts were evaluated for CAR T cell anti-tumor activity (e.g., a decrease in mouse tumors and mouse blood IFNγ, TNFα, et al.).

The term “chimeric antigen receptor” or alternatively a “CAR” refers to a recombinant polypeptide construct comprising at least an extracellular antigen binding domain, a transmembrane domain and an intracellular signaling domain (e.g., cytoplasmic domain). In embodiments, the domains in the CAR polypeptide construct are on the same polypeptide chain (e.g., comprising a chimeric fusion protein). In embodiments, the domains of the CAR polypeptide are not on the same molecule, e.g. not contiguous with each other or are on different polypeptide chains.

In embodiments, the intracellular signaling domain may include a functional signaling domain derived from a stimulatory molecule and/or a co-stimulatory molecule as described herein. In embodiments, the intracellular signaling domain includes a functional signaling domain derived from a primary signaling domain (e.g., a primary signaling domain of CD3-zeta). In embodiments, the intracellular signaling domain further includes one or more functional signaling domains derived from at least one co-stimulatory molecule. The co-stimulatory signaling region refers to a portion of the CAR including the intracellular domain of a co-stimulatory molecule. Co-stimulatory molecules can include cell surface molecules for inducing an efficient response from the lymphocytes (in response to an antigen).

Between the extracellular domain and the transmembrane domain of the CAR, there may be incorporated a spacer domain. As used herein, the term “spacer domain” generally means any oligo- or polypeptide that functions to link the transmembrane domain to the extracellular domain and/or the cytoplasmic domain in the polypeptide chain. A spacer domain may include up to 300 amino acids, 10 to 100 amino acids, or 25 to 50 amino acids.

The extracellular domain of a CAR may include an antigen binding domain (e.g., a scFv, a single domain antibody, or TCR, such as a TCR alpha binding domain or a TCR beta binding domain) that targets a specific tumor marker (e.g., a tumor antigen). Tumor antigens are proteins that are produced by tumor cells that elicit an immune response, particularly T cell mediated immune responses. Tumor antigens are well known in the art and include, for example, a glioma-associated antigen, carcinoembryonic antigen (CEA), β-human chorionic gonadotropin, alphafetoprotein (AFP), lectin-reactive AFP, thyroglobulin, RAGE-1, MN-CA IX, human telomerase reverse transcriptase, RU1, RU2 (AS), intestinal carboxyl esterase, mut hsp70-2, M-CSF, prostase, prostate-specific antigen (PSA), PAP, NY-ESO-1, LAGE-1a, p53, prostein, PSMA, Her2/neu, survivin and telomerase, prostate-carcinoma tumor antigen-1 (PCTA-1), MAGE, ELF2M, neutrophil elastase, ephrinB2, CD22, insulin growth factor (IGF)-I, IGF-II, IGF-I receptor and mesothelin. For example, when the antigen that the CAR binds is CD19, the CAR thereof is referred to as CD19CAR.

In embodiments, the extracellular ligand-binding domain comprises a scFv comprising the light chain variable (VL) region and the heavy chain variable (VH) region of a target antigen-specific monoclonal antibody joined by a flexible linker. Single chain variable region fragments are made by linking light and/or heavy chain variable regions by using a short linking peptide (Bird et al., Science 242:423-426, 1988). An example of a linking peptide is the GS linker having the amino acid sequence (GGGGS)3 (SEQ ID: 24), which bridges approximately 3.5 nm between the carboxy terminus of one variable region and the amino terminus of the other variable region. Linkers of other sequences have been designed and used (Bird et al., 1988, supra). In general, linkers can be short, flexible polypeptides comprising about 20 or fewer amino acid residues. Linkers can in turn be modified for additional functions, such as attachment of drugs or attachment to solid supports. The single chain variants can be produced either recombinantly or synthetically. For synthetic production of scFv, an automated synthesizer can be used. For recombinant production of scFv, a suitable plasmid containing polynucleotide that encodes the scFv can be introduced into a suitable host cell, either eukaryotic, such as yeast, plant, insect or mammalian cells, or prokaryotic, such as E. coli. Polynucleotides encoding the scFv of interest can be made by routine manipulations such as ligation of polynucleotides. The resultant scFv can be isolated using standard protein purification techniques known in the art.

In embodiments, the tumor antigen includes HER2, CD19, CD20, CD22, Kappa or light chain, CD30, CD33, CD123, CD38, ROR1, ErbB3/4, EGFR, EGFRvIII, EphA2, FAP, carcinoembryonic antigen, EGP2, EGP40, mesothelin, TAG72, PSMA, NKG2D ligands, B7-H6, IL-13 receptor α 2, IL-11 receptor α, MUC1, MUC16, CA9, GD2, GD3, HMW-MAA, CD171, Lewis Y, G250/CAIX, HLA-AI MAGE A1, HLA-A2 NY-ESO-1, PSC1, folate receptor-α, CD44v7/8, 8H9, NCAM, VEGF receptors, 5T4, Fetal AchR, NKG2D ligands, CD44v6, TEM1, TEM8, or viral-associated antigens expressed by a tumor. In embodiments, the binding element of the CAR may include any antigen binding moiety that when bound to its cognate antigen, affects a tumor cell such that the tumor cell fails to grow, or is promoted to die or diminish.

In embodiments, the extracellular domain of the CAR binds KISS1R. KISS1R is a galanin-like G protein-coupled receptor that binds Kisspeptin (metastin), a peptide encoded by the metastasis suppressor gene KISS1. KISS1 R may be involved in the regulation of endocrine function. For example, the extracellular domain of the CAR binds KISS1R having the amino acid sequence of SEQ ID NO: 19. In embodiments, the extracellular domain of the CAR comprises one of the amino acid sequences of SEQ ID NOs: 71 and 72. Embodiments relate to a method of eliciting and/or enhancing T cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with renal cancer.

In embodiments, the extracellular domain of the CAR binds CLDN6. CLDN6 is a component of tight junction strands, which is a member of the claudin family, an integral membrane protein. Transcriptional data predict high expression in endometrial cancer, urothelial cancer, whereas expression in normal tissues is a component of tight junction strands, which are members of the claudin family Low volume. For example, the extracellular domain of the CAR binds CLDN6 having the amino acid sequence of SEQ ID NO: 22. In embodiments, the extracellular domain of the CAR comprises one of the amino acid sequences of SEQ ID NOs: 29-44. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with endometrial cancer and/or urothelial cancer.

In embodiments, the extracellular domain of the CAR binds MUC16. MUC21 and MUC16 are large membrane-bound glycoproteins, which belong to mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. MUC21 has restricted expression toward esophagus, for esophageal cancer. MUC16 has low expression in normal tissues and low expression in the endometrium. In ovarian cancer, MUC16 is highly expressed. For example, the extracellular domain of the CAR binds MUC16 having the amino acid sequence of SEQ ID NO: 6. In embodiments, the extracellular domain of the CAR comprises one of the amino acid sequences of SEQ ID NOs: 63-70. Embodiments relate to a method of eliciting and/or enhancing T cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with ovarian cancer.

In embodiments, the extracellular domain of the CAR binds SLC6A3. SLC6A3 is a dopamine transporter, a member of the sodium- and chloride-dependent neurotransmitter transporter family. For example, the extracellular domain of the CAR binds SLC6A3 having the amino acid sequence of SEQ ID NO: 18. Embodiments include a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor comprises renal cancer.

In embodiments, the extracellular domain of the CAR binds QRFPR. QRFPR is pyroglutamylated RFamide peptide receptor and may be involved in adipogenesis with its ligand, QRFP. For example, the extracellular domain of the CAR binds QRFPR having the amino acid sequence of SEQ ID NO: 20. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with renal cancer.

In embodiments, the extracellular domain of the CAR binds GPR119. GPR119 is a member of the rhodopsin subfamily of G-protein-coupled receptors, has low expression in the pancreas and gastrointestinal tract, and may be involved in glucose homeostasis. Transcriptional data predict high expression in pancreatic cancer. For example, the extracellular domain of the CAR binds GPR119 having the amino acid sequence of SEQ ID NO: 21. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor of the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with pancreatic cancer.

In embodiments, the extracellular domain of the CAR bindsUPK2. UPK2 is one of the proteins of the highly conserved urothelium-specific integral membrane proteins of the asymmetric unit membrane, expressed primarily in urinary bladder in normal tissues and urothelial carcinoma, including bladder cancer. For example, the extracellular domain of the CAR binds UPK2 having the amino acid sequence of SEQ ID NO: 1. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with urothelial cancer and/or bladder cancer.

In embodiments, the extracellular domain of the CAR binds ADAM12. ADAM12 is a member of a family of proteins that are structurally related to snake venom disintegrins, involved in cell-cell and cell-matrix interactions, and is highly expressed in tumors such as placenta and breast/pancreatic cancer. For example, the extracellular domain of the CAR binds ADAM12 having the amino acid sequence of SEQ ID NO: 2. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with breast cancer and/or pancreatic cancer.

In embodiments, the extracellular domain of the CAR binds SLC45A3. SLC45A3 is a plasma membrane protein, normal tissue is mainly expressed in prostate, for prostate cancer. For example, the extracellular domain of the CAR binds SLC45A3 having the amino acid sequence of SEQ ID NO: 3. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with prostate cancer.

In embodiments, the extracellular domain of the CAR binds ACPP. ACPP is an enzyme that catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate, contains a transmembrane domain and localized in the plasma membrane-endosomal-lysosomal pathway. Normal tissue is specifically expressed in the prostate for prostate cancer. For example, the extracellular domain of the CAR binds ACPP having the amino acid sequence of SEQ ID NO: 4. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with prostate cancer.

In embodiments, the extracellular domain of the CAR binds MUC21. MUC21 and MUC16 are large membrane-bound glycoproteins, which belong to mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. MUC21 has restricted expression toward esophagus, when the subject has esophageal cancer. For example, the extracellular domain of the CAR binds MUC21 having the amino acid sequence of SEQ ID NO: 5. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with esophageal cancer.

In embodiments, the extracellular domain of the CAR binds MS4A12. MS4A12 is a cell surface protein found in the apical membrane of colonocytes, restricted expression on colon, and may be used against colorectal cancer. For example, the extracellular domain of the CAR binds MS4A12 having the amino acid sequence of SEQ ID NO: 7. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with colorectal cancer.

In embodiments, the extracellular domain of the CAR binds ALPP. ALPP is an alkaline phosphatase, a metalloenzyme that catalyzes the hydrolysis of phosphoric acid monoesters. The expression of ALPP is restricted to the placenta, Strong ectopic expression of ALPP has been detected in ovarian adenocarcinoma, serous cystadenocarcinoma, and other ovarian cancer cells. For example, the extracellular domain of the CAR binds ALPP having the amino acid sequence of SEQ ID NO: 8. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the solid tumor is associated with endometrial cancer.

In embodiments, the extracellular domain of the CAR binds SLC2A14. For example, the extracellular domain of the CAR binds SLC2A14 having the amino acid sequence of SEQ ID NO: 9. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with testicular cancer.

In embodiments, the extracellular domain of the CAR binds GS1-259H13.2. For example, the extracellular domain of the CAR binds GS1-259H13.2 having the amino acid sequence of SEQ ID NO: 10. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor of the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with thyroid cancer or glioma, or testicular cancer.

In embodiments, the extracellular domain of the CAR binds ERVFRD-1. For example, the extracellular domain of the CAR binds ERVFRD-1 having the amino acid sequence of SEQ ID NO: 11. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with kidney cancer or Urethral cancer.

In embodiments, the extracellular domain of the CAR binds ADGRG2. For example, the extracellular domain of the CAR binds ADGRG2 having the amino acid sequence of SEQ ID NO: 12. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject havinga solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with ovarian cancer.

In embodiments, the extracellular domain of the CAR binds ECEL1. For example, the extracellular domain of the CAR binds ECEL1 having the amino acid sequence of SEQ ID NO: 13. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with endometrial cancer.

In embodiments, the extracellular domain of the CAR binds CHRNA2. For example, the extracellular domain of the CAR binds CHRNA2 having the amino acid sequence of SEQ ID NO: 14. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with prostate cancer.

In embodiments, the extracellular domain of the CAR binds GP2. For example, the extracellular domain of the CAR binds GP2 having the amino acid sequence of SEQ ID NO: 15. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with pancreatic cancer.

In embodiments, the extracellular domain of the CAR binds PSG9. For example, the extracellular domain of the CAR binds PSG9 having the amino acid sequence of SEQ ID NO: 16. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, wherein the method comprises administering an effective amount of T cells comprising the CAR. In embodiments, the tumor is associated with Kidney cancer or liver cancer.

The present disclosure also relates to a bispecific chimeric antigen receptor (See FIG. 26), a polynucleotide encoding the bispecific chimeric antigen receptor, and/or a modified cell comprising the polynucleotide, wherein the bispecific chimeric antigen receptor comprises a first antigen binding domain, a second antigen binding domain, a cytoplasmic domain, and a transmembrane domain, and wherein the first antigen binding domain recognizes a first antigen, and the second antigen binding domain recognize a second antigen. In embodiments, the first antigen is an antigen associated with a white blood cell, and the second antigen is a solid tumor antigen. In embodiments, the first and second antigens are identical or different. In embodiments, the first and second antigens are both solid tumor antigens. For example, the first antigen is a tumor associated MUC1, and the second antigen is selected from one of the antigens of SEQ ID NO: 1-22. In embodiments, the first binding domain and the second binding domain are connected via a linker (e.g., SEQ ID NO: 188).

In embodiments, the intracellular domain of the CAR comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1 BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof.

In embodiments, the intracellular domain comprises a CD3 zeta signaling domain. Embodiments relate to a vector comprising the isolated nucleic acid sequence described herein. Embodiments relate to an isolated cell comprising the isolated nucleic acid sequence described herein.

Embodiments relate to a composition comprising a population of cells including T cells comprising the CAR described herein. Embodiments relate to a CAR encoded by the isolated nucleic acid sequence described herein.

The cells, including CAR cells and modified cells, described herein can be derived from a stem cell. The stem cells may be adult stem cells, embryonic stem cells, or non-human stem cells, cord blood stem cells, progenitor cells, bone marrow stem cells, induced pluripotent stem cells, totipotent stem cells, or hematopoietic stem cells. The cells can also be a dendritic cell, a NK-cell, a B-cell, or a T cell selected from the group consisting of inflammatory T lymphocytes, cytotoxic T lymphocytes, regulatory T lymphocytes, and helper T lymphocytes. In embodiments, the cells can be derived from the group consisting of CD4+T-lymphocytes and CD8+T-lymphocytes. Prior to expansion and genetic modification of the cells described herein, a source of cells may be obtained from a subject through a variety of non-limiting methods. T cells may be obtained from a number of non-limiting sources, including peripheral blood mononuclear cells, bone marrow, lymph node tissue, cord blood, thymus tissue, tissue from a site of infection, ascites, pleural effusion, spleen tissue, and tumors. In embodiments, any number of T cell lines available and known to those skilled in the art, can be used. In embodiments, the cells may be derived from a healthy donor, from a patient diagnosed with cancer or from a patient diagnosed with an infection. In embodiments, the cells are part of a mixed population of cells which present different phenotypic characteristics.

The term “stem cell” refers to any type of cell which has the capacity for self-renewal and the ability to differentiate into other kind(s) of cell. For example, a stem cell gives rise either to two daughter stem cells (as occurs in vitro with embryonic stem cells in culture) or to one stem cell and a cell that undergoes differentiation (as occurs e.g. in hematopoietic stem cells, which give rise to blood cells). Different categories of stem cells may be distinguished on the basis of their origin and/or on the extent of their capacity for differentiation into other types of cell. Stem cells can include embryonic stem (ES) cells (i.e., pluripotent stem cells), somatic stem cells, induced pluripotent stem cells, and any other types stem cells.

Pluripotent embryonic stem cells can be found in the inner cell mass of a blastocyst and have high innate capacity for differentiation. For example, pluripotent embryonic stem cells have the potential to form any type of cell in the body. When grown in vitro for long periods of time, ES cells maintain pluripotency, and progeny cells retain the potential for multilineage differentiation.

Somatic stem cells can include fetal stem cells (from the fetus) and adult stem cells (found in various tissues, such as bone marrow). These cells have been regarded as having a capacity for differentiation lower than that of the pluripotent ES cells—with the capacity of fetal stem cells being greater than that of adult stem cells; they apparently differentiate into only a limited number of different types of cells and have been described as multipotent. “Tissue-specific” stem cells normally give rise to only one type of cell. For example, embryonic stem cells can differentiate into blood stem cells (e.g., Hematopoietic stem cells (HSCs)), which can further differentiate into various blood cells (e.g., red blood cells, platelets, white blood cells, etc.).

Induced pluripotent stem cells (iPS cells or iPSCs) can include a type of pluripotent stem cell artificially derived from a non-pluripotent cell (e.g., an adult somatic cell) by inducing expression of specific genes. Induced pluripotent stem cells are similar to naturally occurring pluripotent stem cells, such as embryonic stem (ES) cells, in many aspects, such as the expression of certain stem cell genes and proteins, chromatin methylation patterns, doubling time, embryoid body formation, teratoma formation, viable chimera formation, and potency and differentiability. Induced pluripotent cells can be isolated from adult stomach, liver, skin cells, and blood cells.

In embodiments, the CAR cells, the modified cell, or the cell is a T cell, a NK cell, a macrophage or a dendritic cell. For example, the CAR cells, the modified cell, or the cell is a T cell.

In embodiments, the antigen binding molecule is a T Cell Receptor (TCR). In embodiments, the TCR is modified TCR. In embodiments, the TCR is derived from spontaneously occurring tumor-specific T cells in patients. In embodiments, the TCR binds a tumor antigen. In embodiments, the tumor antigen comprises CEA, gp100, MART-1, p53, MAGE-A3, or NY-ESO-1. In embodiments, the TCR comprises TCRγ and TCRδ chains or TCRα and TCRβ chains. In embodiments, a T cell clone that expresses a TCR with high affinity for the target antigen may be isolated. In embodiments, tumor-infiltrating lymphocytes (TILs) or peripheral blood mononuclear cells (PBMCs) may be cultured in the presence of antigen-presenting cells (APCs) pulsed with a peptide representing an epitope known to elicit a dominant T cell response when presented in the context of a defined HLA allele. High-affinity clones may be then selected on the basis of MHC-peptide tetramer staining and/or the ability to recognize and lyse target cells pulsed with low titrated concentrations of cognate peptide antigen. After the clone has been selected, the TCRα and TCRβ chains or TCRγ and TCRδ chains are identified and isolated by molecular cloning. For example, for TCRα and TCRβ chains, the TCRα and TCRβ gene sequences are then used to generate an expression construct that ideally promotes stable, high-level expression of both TCR chains in human T cells. The transduction vehicle (e.g., a gammaretrovirus or lentivirus) may be then generated and tested for functionality (antigen specificity and functional avidity) and used to produce a clinical lot of the vector. An aliquot of the final product is then used to transduce the target T cell population (generally purified from patient PBMCs), which is expanded before infusion into the subject.

In embodiments, the binding element of the CAR may include any antigen binding moiety that when bound to its cognate antigen, affects a tumor cell for example, it kills the tumor cell, inhibits the growth of the tumor cell, or promotes death of the tumor cell.

The nucleic acid sequences coding for the desired molecules can be obtained using recombinant methods known in the art, such as, for example by screening libraries from cells expressing the gene, by deriving the gene from a vector known to include the same, or by isolating directly from cells and tissues containing the same, using standard techniques. Alternatively, the gene of interest can be produced synthetically, rather than cloned.

The embodiments of the present disclosure further relate to vectors in which a DNA of the present disclosure is inserted. Vectors derived from retroviruses such as the lentivirus are suitable tools to achieve long-term gene transfer since they allow long-term, stable integration of a transgene and its propagation in daughter cells. Lentiviral vectors have the added advantage over vectors derived from onco-retroviruses such as murine leukemia viruses in that they can transduce non-proliferating cells, such as hepatocytes. They also have the added advantage of low immunogenicity.

Viruses can be used to deliver nucleic acids into a cell in vitro and in vivo (in a subject). Examples of viruses useful for delivery of nucleic acids into cells include retrovirus, adenovirus, herpes simplex virus, vaccinia virus, and adeno-associated virus.

There also exist non-viral methods for delivering nucleic acids into a cell, for example, electroporation, gene gun, sonoporation, magnetofection, and the use of oligonucleotides, lipoplexes, dendrimers, and inorganic nanoparticles.

The expression of natural or synthetic nucleic acids encoding CARs is typically achieved by operably linking a nucleic acid encoding the CAR polypeptide or portions thereof to one or more promoters and incorporating the construct into an expression vector. The vectors can be suitable for replication and integration into eukaryotes. Typical cloning vectors contain transcription and translation terminators, initiation sequences, and promoters useful for regulation of the expression of the desired nucleic acid sequence.

Additional information related to expression of synthetic nucleic acids encoding CARs and gene transfer into mammalian cells is provided in U.S. Pat. No. 8,906,682, incorporated by reference in its entirety.

Pharmaceutical compositions of the present disclosure may be administered in a manner appropriate to the disease to be treated (or prevented). The quantity and frequency of administration will be determined by such factors as the condition of the patient, and the type and severity of the patient's disease, although appropriate dosages may be determined by clinical trials.

When “an immunologically effective amount”, “an anti-tumor effective amount”, “a tumor-inhibiting effective amount”, or “therapeutic amount” is indicated, the precise amount of the compositions of the present disclosure to be administered can be determined by a physician with consideration of individual differences in age, weight, tumor size, extent of infection or metastasis, and condition of the patient (subject). It can be stated that a pharmaceutical composition comprising the T cells described herein may be administered at a dosage of 10⁴ to 10⁹ cells/kg body weight, preferably 10⁵ to 10⁶ cells/kg body weight, including all integer values within those ranges. T cell compositions may also be administered multiple times at these dosages. The cells can be administered by using infusion techniques that are commonly known in immunotherapy (see, e.g., Rosenberg et al., New Eng. J. of Med. 319:1676, 1988). The optimal dosage and treatment regime for a particular patient can readily be determined by one skilled in the art of medicine by monitoring the patient for signs of disease and adjusting the treatment accordingly. In embodiments, it may be desired to administer activated T cells to a subject and then subsequently redraw the blood (or have apheresis performed), collect the activated and expanded T cells, and reinfuse the patient with these activated and expanded T cells. This process can be carried out multiple times every few weeks. In embodiments, T cells can be activated from blood draws of from 10 cc to 400 cc. In embodiments, T cells are activated from blood draws of 20 cc, 30 cc, 40 cc, 50 cc, 60 cc, 70 cc, 80 cc, 90 cc, or 100 cc. Not to be bound by theory, using this multiple blood draw/multiple reinfusion protocols, certain populations of T cells may be selected.

The administration of the pharmaceutical compositions described herein may be carried out in any convenient manner, including by aerosol inhalation, injection, ingestion, transfusion, implantation or transplantation. The compositions described herein may be administered to a patient subcutaneously, intradermally, intratumorally, intranodally, intramedullary, intramuscularly, by intravenous (i. v.) injection, or intraperitoneally. In embodiments, the T cell compositions of the present disclosure are administered to a patient by intradermal or subcutaneous injection. In embodiments, the T cell compositions of the present disclosure are preferably administered by i.v. injection. The compositions of T cells may be injected directly into a tumor, lymph node, or site of infection. In embodiments of the present disclosure, cells activated and expanded using the methods described herein, or other methods known in the art where T cells are expanded to therapeutic levels, are administered to a patient in conjunction with (e.g., before, simultaneously or following) any number of relevant treatment modalities, including but not limited to treatment with agents such as antiviral therapy, cidofovir and interleukin-2, Cytarabine (also known as ARA-C) or natalizumab treatment for MS patients or efalizumab treatment for psoriasis patients or other treatments for PML patients. In further embodiments, the T cells of the present disclosure may be used in combination with chemotherapy, radiation, immunosuppressive agents, such as cyclosporin, azathioprine, methotrexate, mycophenolate, and FK506, antibodies, or other immunoablative agents such as CAM PATH, anti-CD3 antibodies or other antibody therapies, cytoxin, fludaribine, cyclosporin, FK506, rapamycin, mycophenolic acid, steroids, FR901228, cytokines, and irradiation. These drugs inhibit either the calcium dependent phosphatase calcineurin (cyclosporine and FK506) or inhibit the p70S6 kinase that is important for growth factor induced signaling (rapamycin). (Liu et al., Cell 66:807-815, 1991; Henderson et al., Immun 73:316-321, 1991; Bierer et al., Curr. Opin. Immun 5:763-773, 1993; Isoniemi (supra)). In embodiments, the cell compositions of the present disclosure are administered to a patient in conjunction with (e.g., before, simultaneously or following) bone marrow transplantation, T cell ablative therapy using either chemotherapy agents such as, fludarabine, external-beam radiation therapy (XRT), cyclophosphamide, or antibodies such as OKT3 or CAMPATH. In embodiments, the cell compositions of the present disclosure are administered following B-cell ablative therapy such as agents that react with CD20, e.g., Rituxan. For example, subjects may undergo standard treatment with high dose chemotherapy followed by peripheral blood stem cell transplantation. In embodiments, following the transplant, subjects receive an infusion of the expanded immune cells of the present disclosure. In embodiments, expanded cells are administered before or following surgery.

The dosage of the above treatments to be administered to a patient will vary with the precise nature of the condition being treated and the recipient of the treatment. The scaling of dosages for human administration can be performed according to art-accepted practices by a physician depending on various factors.

Additional information on the methods of cancer treatment using engineered or modified T cells is provided in U.S. Pat. No. 8,906,682, incorporated by reference in its entirety.

In embodiments, the population of cells described herein is used in autologous CAR T cell therapy. In embodiments, the CAR T cell therapy is allogenic CAR T cell therapy, TCR T cell therapy, and NK cell therapy.

Embodiments relate to an in vitro method for preparing modified cells. The method may include obtaining a sample of cells from the subject. For example, the sample may include T cells or T cell progenitors. The method may further include transfecting the cells with a DNA encoding at least a CAR, culturing the population of CAR cells ex vivo in a medium that selectively enhances proliferation of CAR-expressing T cells.

In embodiments, the sample is a cryopreserved sample. In embodiments, the sample of cells is from umbilical cord blood or a peripheral blood sample from the subject. In embodiments, the sample of cells is obtained by apheresis or venipuncture. In embodiments, the sample of cells is a subpopulation of T cells.

Embodiments of the present disclosure relate to treating cancer using Chimeric Antigen Receptor (CAR) cells using a molecule associated with a gene fusion. Embodiments relate to an isolated nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, wherein the extracellular domain binds a gene fusion antigen of a gene fusion.

As used herein, the term “gene fusion” refers to the fusion of at least a portion of a gene to at least a portion of an additional gene. The gene fusion need not include entire genes or exons of genes. In some instances, gene fusion is associated with alternations in cancer. A gene fusion product refers to a chimeric genomic DNA, a chimeric messenger RNA, a truncated protein or a chimeric protein resulting from a gene fusion. The gene fusion product may be detected by various methods described in U.S. Pat. No. 9,938,582, which is incorporated as a reference herein. A “gene fusion antigen” refers to a truncated protein or a chimeric protein that results from a gene fusion. In embodiments, an epitope of a gene fusion antigen may include a part of the gene fusion antigen or an immunogenic part of another antigen caused by the gene fusion. In embodiments, the gene fusion antigen interacts with, or is part of, cell membranes.

In embodiments, the gene fusion comprises a fusion of at least a portion of a first gene to at least a portion of a second gene. In embodiments, the first gene and the second gene comprise a first gene and a second gene of a fusion listed in Table 3. In embodiments, the gene fusion antigen is associated with a condition listed in the Table 3.

In embodiments, detection of mRNA and protein expression levels of the target molecules (listed in Table 2) in human cells may be performed using experimental methods such as qPCR and FACS. Further, target molecules specifically expressed in the corresponding tumor cells with very low expression or undetectable expression in normal tissue cells may be identified.

In embodiments, In Vitro Killer Assay as well as killing experiment of CAR T Cells Co-Cultured with Antigen-Positive Cells may be performed. CAR T cells may exhibit a killing effect on the corresponding antigen-positive cells, a decrease in the number of corresponding antigen-positive cells co-cultured with CAR T cells, and an increase in the release of IFNγ, TNFα, etc. as compared to control cells that did not express the corresponding antigen.

In embodiments, In Vivo Killer Assay may be performed. For example, mice may be transplanted with corresponding antigen tumor cells, and tumorigenic, transfusion of CAR T cells, and a decrease in mouse tumors and mouse blood IFNγ, TNFα, and other signals may be defected.

Embodiments relate to a method of eliciting and/or enhancing T cell response in a subject having a solid tumor or treating a solid tumor in the subject, the method comprising administering an effective amount of T cells comprising the CAR described herein. In embodiments, the intracellular domain of the CAR comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1 BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. In embodiments, the intracellular domain comprises a CD3 zeta signaling domain.

Embodiments relate to a vector comprising the isolated nucleic acid described herein.

Embodiments relate to an isolated cell comprising the isolated nucleic acid sequence described herein. Embodiments relate to a composition comprising a population of T cells comprising the CAR described herein. Embodiments relate to a CAR encoded by the isolated nucleic acid sequence described herein. Embodiments relate to a method of eliciting and/or enhancing T-cell response in a subject or treating a tumor of the subject, the method comprising: administering an effective amount of T cell comprising the CAR described herein.

TABLE 3 Second Conditions Type Fusion First gene Gene description sublocation Gene Gene description sublocation breast invasive BRC GNAS-- GNAS GNAS complex Plasma NECTIN2 Nectin cell Plasma carcinoma A NECTIN2 locus membrane adhesion molecule membrane 2 breast invasive BRC FGFR1-- FGFR1 Fibroblast growth Plasma ADAM18 ADAM Plasma carcinoma A ADAM18 factor receptor 1 membrane metallopeptidase membrane domain 18 cervical CES WHRN-- WHRN Whirlin Cytoplasm; TNC Tenascin C Extracellular; squamous cell C TNC Plasma Plasma carcinoma and membrane membrane endocervical adenocarcinoma head and neck HNS PQLC1-- PQLC1 PQ loop repeat Plasma HSBP1L1 Heat shock factor Plasma squamous cell C HSBP1L1 containing 1 membrane binding protein 1 membrane carcinoma like 1 kidney renal KIRP FNDC3B-- FNDC3B Fibronectin type Plasma BCHE Butyryl- Plasma papillary cell BCHE III domain membrane cholinesterase membrane carcinoma containing 3B brain lower grade LGG GRIA4-- GRIA4 Glutamate Plasma NAALAD N-acetylated alpha- Plasma glioma NAALAD2 ionotropic membrane 2 linked acidic membrane receptor AM PA dipeptidase 2 type subunit 4 brain lower grade LGG EPHB2-- EPHB2 EPH receptor B2 Plasma PDZD4 PDZ domain Cytoplasm; glioma PDZD4 membrane containing 4 Plasma membrane brain lower grade LGG SEC24A-- SEC24A SEC24 homolog Plasma KCNK7 Potassium two pore Plasma glioma KCNK7 A, COPII coat membrane domain channel membrane complex subfamily K component member 7 liver LIHC ACVR1B-- ACVR1B Activin A receptor Plasma ACVRL1 Activin A receptor Plasma hepatocellular ACVRL1 type 1B membrane like type 1 membrane carcinoma liver LIHC ABCC2-- ABCC2 ATP binding Plasma CTNNA3 Catenin alpha 3 Cytoplasm; hepatocellular CTNNA3 cassette membrane Cytoskeleton; carcinoma subfamily C Plasma member 2 membrane liver LIHC EFNA1-- EFNA1 Ephrin A1 Extracellular; ADAM15 ADAM Plasma hepatocellular ADAM15 Plasma metallopeptidase membrane carcinoma membrane domain 15 lung LUAD CPNE8-- CPNE8 Copine 8 Plasma CADM2 Cell adhesion Plasma adenocarcinoma CADM2 membrane molecule 2 membrane lung LUAD NOTCH2-- NOTCH2 Notch 2 Plasma ADAM30 ADAM Plasma adenocarcinoma ADAM30 membrane metallopeptidase membrane domain 30 lung LUAD CELSR1-- CELSR1 Cadherin EGF Plasma CD52 CD52 molecule Plasma adenocarcinoma CD52 LAG seven-pass membrane membrane G-type receptor 1 lung LUAD ILVBL-- ILVBL IIvB acetolactate Plasma SLC1A6 Solute carrier family Plasma adenocarcinoma SLC1A6 synthase like membrane 1 member 6 membrane lung LUAD F11R-- F11R F11 receptor Plasma NOS1AP Nitric oxide Cytoplasm; adenocarcinoma NOS1AP membrane synthase 1 adaptor Plasma protein membrane lung squamous LUSC CELSR1-- CELSR1 Cadherin EGF Plasma SEZ6L Seizure related 6 Plasma cell carcinoma SEZ6L LAG seven-pass membrane homolog like membrane G-type receptor 1 lung squamous LUSC KIRREL-- KIRREL Kin of IRRE like Plasma CD1A CD1a molecule Endosome; cell carcinoma CD1A (Drosophila) membrane Golgi apparatus; Plasma membrane lung squamous LUSC ATP10D-- ATP10D ATPase Plasma GABRA2 Gamma- Plasma cell carcinoma GABRA2 phospholipid membrane aminobutyric acid membrane transporting 10D type A receptor (putative) alpha2 subunit pancreatic PAA ORAI2-- ORAI2 ORAI calcium Plasma SLC47A2 Solute carrier family Plasma adenocarcinoma D SLC47A2 release-activated membrane 47 member 2 membrane calcium modulator 2 pheochro- PCP ADCYAP1R ADCYAP1R ADCYAP Plasma GHRHR Growth hormone Plasma mocytoma and G 1--GHRHR 1 receptor type I membrane releasing hormone membrane paraganglioma receptor pheochro- PCP TMEM178B-- TMEM178B Transmembrane Plasma DPP6 Dipeptidyl Plasma mocytoma and G DPP6 protein 178B membrane peptidase like 6 membrane paraganglioma prostate PRA ADAM9-- ADAM9 ADAM Plasma RGS20 Regulator of G- Plasma adenocarcinoma D RGS20 metallopeptidase membrane protein signaling 20 membrane domain 9 prostate PRA FAM160B1-- FAM160B1 Family with Plasma VTI1A Vesicle transport Plasma adenocarcinoma D VTI1A sequence membrane through interaction membrane similarity 160 with t-SNAREs 1A member B1 prostate PRA TMPRSS2-- TMPRSS2 Transmembrane Plasma PDE9A Phosphodiesterase Plasma adenocarcinoma D PDE9A protease, serine membrane 9A membrane 2 prostate PRA PDE9A-- PDE9A Phosphodiesterase Plasma TMPRSS Transmembrane Plasma adenocarcinoma D TMPRSS2 9A membrane 2 protease, serine 2 membrane rectum REA LHFPL2-- LHFPL2 Lipoma HMGIC Plasma PTPRK Protein tyrosine Plasma adenocarcinoma D PTPRK fusion partner-like membrane phosphatase, membrane 2 receptor type K sarcoma SAR TM7SF3-- TM7SF3 Transmembrane Plasma KCNC2 Potassium voltage- Plasma C KCNC2 7 superfamily membrane gated channel membrane member 3 subfamily C member 2 sarcoma SAR MPZL1-- MPZL1 Myelin protein Plasma TNFSF4 Tumor necrosis Plasma C TNFSF4 zero like 1 membrane factor superfamily membrane member 4 sarcoma SAR GNG7-- GNG7 G protein subunit Plasma PAQR5 Progestin and Plasma C PAQR5 gamma 7 membrane adipoQ receptor membrane family member 5 sarcoma SAR KIRREL-- KIRREL Kin of IRRE like Plasma CD1A CD1a molecule Endosome; C CD1A (Drosophila) membrane Golgi apparatus; Plasma membrane sarcoma SAR P2RX5-- P2RX5 Purinergic Plasma TRPV1 Transient receptor Plasma C TRPV1 receptor P2X 5 membrane potential cation membrane channel subfamily V member 1 skin cutaneous SKC PTPRG-- PTPRG Protein tyrosine Plasma SYNPR Synaptoporin Plasma melanoma M SYNPR phosphatase, membrane membrane receptor type G

In embodiments, the CAR molecules described herein comprise one or more complementarity-determining regions (CDRs) for binding an antigen of interest. CDRs are part of the variable domains in immunoglobulins and T cell receptors for binding a specific antigen. There are three CDRs for each variable domain. Since there is a variable heavy domain and a variable light domain, there are six CDRs for binding an antigen. Further since an antibody has two heavy chains and two light chains, an antibody has twelve CDRs altogether for binding antigens. In embodiments, the CAR molecules comprise one or more CDRs of SIGLEC15, SLC6A3, KISS1R, QRFPR, GPR119, CLDN6, UPK2, ADAM12, SLC45A3, ACPP, MUC21, MUC16, MS4A12, or ALPP.

The present disclosure describes modified cells that include one or more different antigen binding domains. The modified cells can include at least two different antigen binding domains: a first antigen binding domain for expanding and/or maintaining the genetically modified cells, and a second antigen binding domain for killing a target cell, such as a tumor cell. For example, the first antigen binding domain binds a surface marker, such as a cell surface molecule of a white blood cell (WBC) (e.g., CD19), and the second antigen binding domain binds a target antigen on tumor cells. In embodiments, the cell surface molecule is a surface antigen of a WBC. In embodiments, the target antigen on tumor cells comprise one or more of SIGLEC15, SLC6A3, KISS1R, QRFPR, GPR119, CLDN6, UPK2, ADAM12, SLC45A3, ACPP, MUC21, MUC16, MS4A12, or ALPP. The at least two antigen binding domains may be located on the same or different modified cells. For example, the modified cells may include a modified cell including a CAR binding CD19, a modified cell including a CAR binding to ACPP, a modified cell including a CAR binding CD19 and ACPP, and/or a modified cell including two CARs that respectively bind CD19 and ACPP. In embodiments, the modified cells may be used to treat a subject having cancer.

In embodiments, the modified cells described herein includes a CAR molecule comprising at least two different antigen binding domains. The CAR molecule can be a bispecific CAR molecule. For example, the two antigen binding domains can be on the same CAR molecule, on different CAR molecules, or on a CAR molecule and T cell receptor (TCR). A single CAR can include at least two different antigen binding domains, or the two different antigen binding domains are each on a separate CAR molecule. The at least two different antigen binding domains can be on the same CAR molecule or different CAR molecules, but in the same modified cell. Moreover, the at least two different antigen binding domains can be on a CAR molecule and a T cell receptor in the same modified cell. In embodiments, the bispecific CAR molecule may include a binding domain binding an antigen of WBC (e.g., CD19) and a binding domain binding a solid tumor antigen. In embodiments, the bispecific CAR molecule may include two binding domains binding two different solid tumor antigens.

In embodiments, the at least two different antigen binding domains are on different CAR molecules which are expressed by different modified cells. Further, the one or more different antigen binding domains are on a CAR molecule and a T cell receptor, which are expressed by different modified cells.

Related sequences are provided in this Application and Innovative Cellular Therapeutics' PCT Patent Applications Nos: PCT/CN2016/075061, PCT/CN2018/08891, and PCT/US19/13068, which are incorporated by reference in their entirety.

The present disclosure is further described by reference to the following exemplary embodiments and examples. These exemplary embodiments and examples are provided for purposes of illustration only and are not intended to be limiting unless otherwise specified. Thus, the present disclosure should in no way be construed as being limited to the following exemplary embodiments and examples, but rather, should be construed to encompass any and all variations which become evident as a result of the teaching provided herein.

EXEMPLARY EMBODIMENTS

The following are exemplary embodiments:

1. An isolated nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, wherein the extracellular domain binds an antigen of a solid tumor. 2. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SIGLEC15. 3. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SIGLEC15 having the amino acid sequence of SEQ ID NO: 17. 4. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain comprises one of the amino acid sequences of SEQ ID NOs: 45-56. 5. A method of eliciting and/or enhancing T-cell response in a subject having a solid tumor or treating a solid tumor in the subject, the method comprising administering an effective amount of T cells comprising the CAR of any one of embodiments 2-4. 6. The isolated nucleic acid sequence or the method of any one of embodiments 1-5, wherein the tumor is associated with urothelial cancer. 7. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds KISS1R. 8. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds KISS1R having the amino acid sequence of SEQ ID NO: 19. 9. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain comprises one of the amino acid sequences of SEQ ID NOs: 71 and 72. 10. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 7-9. 11. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 7-10, wherein the tumor is associated with renal cancer. 12. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds CLDN6. 13. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds CLDN6 having the amino acid sequence of SEQ ID NO: 22. 14. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain comprises one of the amino acid sequences of SEQ ID NOs: 29-44. 15. A method of eliciting and/or enhancing T cell response in a subject having a solid tumor or treating a solid tumor in the subject, the method comprising administering an effective amount of T cells comprising the CAR of any one of embodiments 12-15. 16. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 12-16, wherein the tumor is associated with endometrial cancer and/or urothelial cancer. 17. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MUC16. 18. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MUC16 having the amino acid sequence of SEQ ID NO: 6. 19. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain comprises one of the amino acid sequences of SEQ ID NOs: 63-70. 20. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 17-19. 21. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 17-20, wherein the tumor is associated with ovarian cancer. 22. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC6A3. 23. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC6A3 having the amino acid sequence of SEQ ID NO: 18. 24. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 22 and 23. 25. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 22-24, wherein the tumor is associated with renal cancer. 26. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds QRFPR. 27 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds QRFPR having the amino acid sequence of SEQ ID NO: 20. 28. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 26 and 27. 29. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 26-28, wherein the tumor is associated with renal cancer. 30. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GPR119. 31 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GPR119 having the amino acid sequence of SEQ ID NO: 21. 32. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 30 and 31. 33. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 30-32, wherein the tumor is associated with pancreatic cancer. 34. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds UPK2. 35 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds UPK2 having the amino acid sequence of SEQ ID NO: 1. 36. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 34 and 35. 37. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 34-36, wherein the tumor is associated with urothelial cancer and/or bladder cancer. 38. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ADAM12. 39 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ADAM12 having the amino acid sequence of SEQ ID NO: 2. 40. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 38 and 39. 41. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 38-40, wherein the tumor is associated with breast cancer and/or pancreatic cancer. 42. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC45A3. 43 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC45A3 having the amino acid sequence of SEQ ID NO: 3. 44. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 42 and 43. 45. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 42-44, wherein the tumor is associated with prostate cancer. 46. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ACPP. 47 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ACPP having the amino acid sequence of SEQ ID NO: 4. 48. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 46 and 47. 49. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 46-48, wherein the tumor is associated with prostate cancer. 50. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MUC21. 51 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MUC21 having the amino acid sequence of SEQ ID NO: 5. 52. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 50 and 51. 53. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 50-52, wherein the tumor is associated with esophageal cancer. 54. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MS4A12. 55 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds MS4A12 having the amino acid sequence of SEQ ID NO: 7. 56. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 54 and 55. 57. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 54-56, wherein the tumor is associated with colorectal cancer. 58. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ALPP. 59 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ALPP having the amino acid sequence of SEQ ID NO: 8. 60. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 58 and 59. 61. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 58-60, wherein the tumor is associated with endometrial cancer. 62. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC2A14. 63 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds SLC2A14 having the amino acid sequence of SEQ ID NO: 9. 64. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 62 and 63. 65. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 62-64, wherein the tumor is associated with testicular cancer. 66. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GS1-259H13.2. 67 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GS1-259H13.2 having the amino acid sequence of SEQ ID NO: 10. 68. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 66 and 67. 69. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 66-69, wherein the tumor is associated with thyroid cancer or glioma, or testicular cancer. 70. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ERVFRD-1. 71 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ERVFRD-1 having the amino acid sequence of SEQ ID NO: 11. 72. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 70 and 71. 73. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 70-72, wherein the tumor is associated with kidney cancer or Urethral cancer. 74. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ADGRG2. 75 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ADGRG2 having the amino acid sequence of SEQ ID NO: 12. 76. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 74 and 75. 77. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 74-76, wherein the tumor is associated with ovarian cancer. 78. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ECEL1. 79 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds ECEL1 having the amino acid sequence of SEQ ID NO: 13. 80. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 78 and 29. 81. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 78-80, wherein the tumor is associated with endometrial cancer. 82. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds CHRNA2. 83 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds CHRNA2 having the amino acid sequence of SEQ ID NO: 14. 84. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 82 and 83. 85. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 82-84, wherein the tumor is associated with prostate cancer. 86. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GP2. 87 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds GP2 having the amino acid sequence of SEQ ID NO: 15. 88. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 86 and 87. 89. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 86-88, wherein the tumor is associated with pancreatic cancer. 90. The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds PSG9. 91 The isolated nucleic acid sequence of embodiment 1, wherein the extracellular domain binds PSG9 having the amino acid sequence of SEQ ID NO: 16. 92. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any one of embodiments 90 and 91. 93. The isolated nucleic acid sequence or the method of any one of embodiments 1 and 90-92, wherein the tumor is associated with Kidney cancer or liver cancer. 94. The isolated nucleic acid sequence or the method of any one of embodiments 1-93, wherein the intracellular domain comprising a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1 BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. 95. The isolated nucleic acid sequence or the method of any one of embodiments 1-93, wherein the intracellular domain comprises a CD3 zeta signaling domain. 96. A vector comprising the isolated nucleic acid sequence of any one of embodiments 1-93. 97. An isolated cell comprising the isolated nucleic acid sequence of any one of embodiments 1-93. 98. A composition comprising a population of T cells comprising the CAR of any one of embodiments 96 or 97. 99. A CAR encoded by the isolated nucleic acid sequence of any one of embodiments 1-93. 100. An isolated nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, wherein the extracellular domain binds a gene fusion antigen of a gene fusion. 101. The isolated nucleic acid sequence of claim 100, wherein the gene fusion comprises a fusion of at least a portion of a first gene to at least a portion of a second gene. 102. The isolated nucleic acid sequence of embodiment 101, wherein the first gene and the second gene comprise a first gene and a second gene of a fusion listed in Table 5. 103. The isolated nucleic acid sequence of embodiment 102, wherein the gene fusion antigen is associated with a condition listed in the Table 3. 104. A method of eliciting and/or enhancing T-cell response in a subject having the solid tumor or treating the solid tumor of the subject, the method comprising administering an effective amount of T cell comprising the CAR of any of embodiments 100-103. 105. The isolated nucleic acid sequence or the method of any one of embodiments 100-103, wherein the intracellular domain comprising a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1 BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. 106. The isolated nucleic acid sequence or the method of any one of embodiments 100-103, wherein the intracellular domain comprises a CD3 zeta signaling domain. 107. A vector comprising the isolated nucleic acid sequence of any one of embodiments 100-106. 108. An isolated cell comprising the isolated nucleic acid sequence of any one of embodiments 100-106. 109. A composition comprising a population of T cells comprising the CAR of any one of embodiments 8 or 9. 110. A CAR encoded by the isolated nucleic acid sequence of any one of embodiments 100-106. 111. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-110, wherein the cell or modified cell is a T cell derived from a healthy donor or a subject having cancer, and the modified T cell comprises a dominant negative form of a receptor associated with an immune checkpoint inhibitor. 112. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-110, wherein the immune checkpoint inhibitor is selected from the group consisting of programmed death 1 (PD-1), cytotoxic T lymphocyte antigen-4 (CTLA-4), B- and T-lymphocyte attenuator (BTLA), T cell immunoglobulin mucin-3 (TIM-3), lymphocyte-activation protein 3 (LAG-3), T cell immunoreceptor with Ig and ITIM domains (TIGIT), leukocyte-associated immunoglobulin-like receptor 1 (LAIRI), natural killer cell receptor 2B4 (2B4), and CD 160. 113. The isolated nucleic acid sequence, modified T cell or the method of embodiment 112, wherein immune checkpoint inhibitor is modified PD-1. 114. The isolated nucleic acid sequence, modified T cell or the method of embodiment 112, wherein the modified PD-1 lacks a functional PD-1 intracellular domain for PD-1 signal transduction, interferes with a pathway between PD-1 of a human T cell of the human cells and PD-L1 of a certain cell, comprises or is a PD-1 extracellular domain or a PD-1 transmembrane domain, or a combination thereof, or a modified PD-1 intracellular domain comprising a substitution or deletion as compared to a wild-type PD-1 intracellular domain, or comprises or is a soluble receptor comprising a PD-1 extracellular domain that binds PD-L1 of a certain cell. 115. The isolated nucleic acid sequence, modified T cell or the method of embodiment 112, wherein an inhibitory effect of PD-L1 on cytokine production of the human T cells of the population is less than an inhibitory effect of PD-L1 on cytokine production of human T cells that do not comprise at least a part of the nucleic acid sequence that encodes the modified PD-1. 116. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-104, wherein the modified T cell is engineered to express and secrete a therapeutic agent such as a cytokine. 117. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the therapeutic agent that is or comprises IFN-γ. 118. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the therapeutic agent is or comprises at least one of IL-6 or IFN-γ, IL-17, and CCL19. 119. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the therapeutic agent that is or comprises IL-15 or IL-12, or a combination thereof. 120. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the small protein or the therapeutic agent is or comprises a recombinant or native cytokine. 121. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the therapeutic agent comprises a FC fusion protein associated with a small protein. 122. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the small protein is or comprises IL-12, IL-15, IL-6 or IFN-γ. 123. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the therapeutic agent is regulated by Hif1a, NFAT, FOXP3, and/or NFkB. 124. The isolated nucleic acid sequence, modified T cell or the method of embodiment 116, wherein the small protein or the therapeutic agent is or comprises two or more recombinant or native cytokines are collected via 2A or/IRES component. 125. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-124, wherein the modified T cell comprises a first targeting vector and a second targeting vector, the first targeting vector comprising a nucleic acid sequence encoding a CAR binding a blood antigen and the therapeutic agent, and the second targeting vector comprises a nucleic acid sequence encoding a CAR biding solid tumor antigen and a dominant negative form of the immune checkpoint molecule. 126. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-124, wherein the modified T cell comprises a first targeting vector and a second targeting vector, the first targeting vector comprising a nucleic acid sequence encoding a CAR binding CD19 and the therapeutic agent, and the second targeting vector comprises a nucleic acid sequence encoding a CAR biding UPK2, ACPP, SIGLEC15 or KISS1R and a dominant negative form of PD-1. 127. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-124, wherein the modified T cell comprises a first targeting vector and a second targeting vector, the first targeting vector comprising a nucleic acid sequence encoding a CAR binding a blood antigen, and the second targeting vector comprises a nucleic acid sequence encoding a CAR biding solid tumor antigen. 128. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-124, wherein the modified T cell comprises a first targeting vector and a second targeting vector, the first targeting vector comprising a nucleic acid sequence encoding a CAR binding a B cell antigen, and the second targeting vector comprises a nucleic acid sequence encoding a CAR biding solid tumor antigen. 129. The isolated nucleic acid sequence, modified T cell or the method of embodiment 128, wherein the solid tumor antigen is at least one of antigens listed in Table 2, and/or the B cell antigen is CD19, CD20, CD22, or BCMA. 130. The isolated nucleic acid sequence, modified T cell or the method of embodiment 128, wherein the solid tumor antigen comprises at least one of antigens listed in Table 2. 131. A method of eliciting and/or enhancing T cell expansion in a subject in need thereof, 0 the method comprising administering an effective amount of the composition of T cells of embodiment 130 to the subject, the subject having a higher level of T cell expansion as compared with a subject that is administered an effective amount of the CAR T cells that do not have the CAR binding the B cell antigen. 132. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-131, wherein the modified T cell comprises a nucleic acid sequence encoding hTERT, SV40LT, or a combination thereof. 133. The isolated nucleic acid sequence, modified T cell or the method of embodiment 132, wherein the modified T cell is more proliferable than T cells without nucleic acid sequence. 134. The isolated nucleic acid sequence, modified T cell or the method of embodiment 133, wherein the proliferable cell remains functions of normal T cells/CAR T cells such as cell therapy functions. 135. The isolated nucleic acid sequence, modified T cell or the method of embodiment 133, wherein the T cell comprises a CAR and is cultured in the presence of an agent that is recognized by the extracellular domain of the CAR, thereby producing a modified CAR cell. 136. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-135, wherein integration of the nucleic acid sequence encoding hTERT, the nucleic acid encoding SV40LT, or a combination thereof includes genomic integration of the nucleic acid sequence encoding hTERT, a nucleic acid encoding SV40LT, or a combination thereof and constitutive expression of hTERT, SV40LT, or a combination thereof. 137. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-136, wherein expression of hTERT, SV40LT, or a combination thereof, is regulated by an inducible expression system such as a rtTA-TRE system. 138. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-136, wherein modified T cell comprises a nucleic acid sequence encoding a suicide gene such as a an HSV-TK system. 139. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-138, wherein the cell has a reduced graft-versus-host disease (GVHD) response in a bioincompatible human recipient as compared to the GVHD response of the primary human T cell. 140. The isolated nucleic acid sequence, modified T cell or the method of one of embodiments 1-138, wherein the cell has a reduced expression of endogenous TRAC gene. 141. A antibody that binds ACPP, wherein the antibody comprises a heavy chain variable region (HVR) sequence comprising the amino acid sequence of SEQ ID NO: 83, 87, 89, or 85 and a light chain variable region (LVR) sequence comprising the amino acid sequences of SEQ ID NO: 82, 86, 88, or 84. 142. The antibody of embodiment 141, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 82, and the comprises the amino acid sequence of SEQ ID NO: 83. 143. The antibody of embodiment 141, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 86, and the HVR comprises the amino acid sequence of SEQ ID NO: 87. 144. The antibody of embodiment 141, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 88, and the HVR comprises the amino acid sequence of SEQ ID NO: 89. 145. The antibody of embodiment 141, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 84, and the HVR comprises the amino acid sequence of SEQ ID NO: 85. 146. The antibody of one of embodiments 141-145, wherein the antibody is a scFv comprising the LVR, a linker, and the HVR. 147. The antibody of one of embodiments 141-146, wherein the HVR is joined to a human IgG chain constant region. 148. The antibody of embodiment 147, wherein the human IgG is IgG1 or IgG3. 149. The antibody of one of embodiments 141-146, wherein the antibody is a conjugated to a cytotoxic agent. 150. The antibody of one of embodiments 141-146, wherein the cytotoxic agent is a radioactive isotope or a toxin. 151. The antibody of one of embodiments 141-146, wherein the antibody is conjugated to a sequence derived from 4-1 BB or CD28, or a combination thereof. 152. The antibody of one of embodiments 141-146, wherein the antibody or fragment is produced in HEK293 cells. 153. A composition comprising the antibody or fragment of one of embodiments 141-152 and a pharmaceutically acceptable carrier. 154. An article of manufacture comprising a container and a composition contained therein, wherein the composition comprises the antibody or fragment of one of embodiments 141-152. 155. A polynucleotide that encodes the antibody or fragment of one of embodiments 141-152. 156. An expression vector encoding the antibody or fragment of one of embodiments 141-152. 157. A host cell comprising a nucleic acid of one of embodiments 155 and 156. 158. A method of treating a subject with cancer, comprising administering to the subject a therapeutically effective amount of the antibody or fragment of one of embodiments 141-152. 159. A method of treating a subject having prostate cancer, comprising administering to the subject a therapeutically effective amount of the antibody or fragment of one of embodiments 141-152. 160. A modified cell comprising a chimeric antigen receptor (CAR) comprising an antigen recognition domain comprising the antibody or fragment of one of embodiments 141-152 and an intracellular domain. 161. A method for treating a subject having cancer, the method comprising: administering a modified cell to the subject, wherein the modified cell comprises an antigen recognition domain comprising the antibody or fragment of one of embodiments 141-152 and an intracellular domain. 162. The modified cell or the method of one of embodiments 160 and 161, wherein the modified cell comprises at least one of a B cell, a T cell, an NK cell, an embryonic cell, a dendritic cell or a macrophage. 163. The method of embodiment 162, wherein the genetically modified cell replicates in vivo. 164. The method of embodiment 161, wherein the modified cell forms memory cells in the subject. 165. The method of embodiment 161, wherein the modified cells are administered intravenously to the subject. 166. The method of embodiment 161, wherein the modified cells persist in the subject. 167. The method of embodiment 161, wherein the modified cell is an autologous T cell. 168. A modified cell comprising a nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an ACPP antigen binding domain comprising the amino acid sequence of SEQ ID NO:83 and 82, 87 and 86, 89 and 88, or 85 and 84. 169. The modified cell of embodiment 168, wherein the CAR further comprises a transmembrane domain, and an intracellular domain and a signaling domain of a co-stimulatory molecule. 170. The modified cell of embodiment 169, wherein the intracellular domain comprising a CD3-zeta signaling domain 171. The modified cell of embodiment 169, wherein the antigen binding fragment is a scFv. 172. The modified cell of embodiment 169, wherein the scFv comprises the amino acid sequence of SEQ ID NO:83 and 82. 173. The modified cell of embodiment 169, wherein the scFv comprises the amino acid sequence of SEQ ID NO:87 and 86. 174. The modified cell of embodiment 169, wherein the scFv comprises the amino acid sequence of SEQ ID NO:89 and 88. 175. The human T cell of embodiment 169, wherein the scFv comprises the amino acid sequence of SEQ ID NO:85 and 84. 176. The modified cell of embodiment 167, wherein the T cell comprises a vector that comprises the nucleic acid sequence. 177. The modified cell of embodiment 176, wherein the vector is a lentiviral vector. 178. The modified cell of one of embodiments 168-177, wherein the modified cell comprises an additional CAR, and the additional CAR binds an antigen of a white blood cell. 179. The modified cell of embodiment 178, wherein the antigen of the white blood cell is a B cell antigen. 180. The modified cell of embodiment 179, wherein the antigen of the B cell antigen is CD19, CD20, CD22, or BCMA. 181. The modified cell of one of embodiments 168-180, wherein the modified cell comprises a dominant negative PD-1. 182. The modified cell one of embodiments 168-180, wherein the modified cell comprises a modified PD-1 lacking a functional PD-1 intracellular domain. 183. The modified cell of one of embodiments 168-180, wherein the intracellular domain comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. 184. The modified cell of embodiment 183, wherein the antigen is Epidermal growth factor receptor (EGFR), Variant III of the epidermal growth factor receptor (EGFRvIII), Human epidermal growth factor receptor 2 (HER2), Mesothelin (MSLN), Prostate-specific membrane antigen (PSMA), Carcinoembryonic antigen (CEA), Disialoganglioside 2 (GD2), Interleukin-13Ra2 (IL13Rα2), Glypican-3 (GPC3), Carbonic anhydrase IX (CAIX), L1 cell adhesion molecule (L1-CAM), Cancer antigen 125 (CA125), Cluster of differentiation 133 (CD133), Fibroblast activation protein (FAP), Cancer/testis antigen 1B (CTAG1B), Mucin 1 (MUC1), Folate receptor-α (FR-α), CD19, FZD10, TSHR, PRLR, Muc 17, GUCY2C, CD207, CD3, CD5, B-Cell Maturation Antigen (BCMA), or CD4. 185. The modified cell of one of embodiment 168-184, wherein the modified cell is a T cell, NK cell, or dendritic cells. 186. The modified cell of one of embodiment 168-185, wherein the modified cell further comprises a nucleic acid sequence encoding a therapeutic agent 187. The modified cell of embodiment 186, wherein the therapeutic agent is present in the modified cell in a recombinant DNA construct, in an mRNA, or in a viral vector. 188. The modified cell of embodiment 186, wherein the modified cell comprises a therapeutic agent mRNA encoding the therapeutic agent, and the mRNA is not integrated into the genome of the modified cell. 189. The modified cell of embodiment 186, wherein the modified cell comprises a nucleic acid sequence comprising or the isolated nucleic acid sequence comprises a promoter comprising a binding site for a transcription modulator that modulates the expression and/or secretion of the therapeutic agent in the cell. 190. The modified cell of embodiment 189, wherein the transcription modulator is or includes Hif1a, NFAT, FOXP3, and/or NFkB. 191. The modified cell of embodiment 189, wherein the promoter is responsive to the transcription modulator. 192. The modified cell of embodiment 189, wherein the promoter is operably linked to the nucleic acid sequence encoding the therapeutic agent such that the promoter drives expression and/or secretion of the therapeutic agent in the cell. 193. A pharmaceutical composition comprising the modified cell of one of embodiments 168-53. 194. A method of eliciting and/or enhancing a T cell response in a subject in need thereof and/or treating a tumor of the subject, the method comprising administering an effective amount of the composition of embodiment 193 to the subject. 195. An antibody or antibody fragment that binds UPK2, wherein the antibody or antibody fragment comprises a heavy chain variable region (HVR) sequence comprising the amino acid sequence of SEQ ID NO: 94, 98, 102, 106, 110, 114, 118, or 122 and a light chain variable region (LVR) sequence comprising the amino acid sequences of SEQ ID NO: 93, 97, 101, 105, 109, 113, 117, or 121. 196. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 93, and HVR comprises the amino acid sequences of SEQ ID NO: 94. 197. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 97, and HVR comprises the amino acid sequences of SEQ ID NO: 98. 198. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 101, and HVR comprises the amino acid sequences of SEQ ID NO: 102. 199. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 105, and HVR comprises the amino acid sequences of SEQ ID NO: 106. 200. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 109, and HVR comprises the amino acid sequences of SEQ ID NO: 110. 201. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 113, and HVR comprises the amino acid sequences of SEQ ID NO: 114. 202. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 117, and HVR comprises the amino acid sequences of SEQ ID NO: 118. 203. The antibody or antibody fragment of embodiment 195, wherein the HVR comprises the amino acid sequences of SEQ ID NO: 121, and HVR comprises the amino acid sequences of SEQ ID NO: 122. 204. The antibody or antibody fragment of one of embodiments 195-203, wherein the HVR is joined to a human IgG chain constant region. 205. The antibody or antibody fragment of embodiment 204, wherein the human IgG is IgG1 or IgG3. 206. The antibody or antibody fragment of one of embodiments 195-205, wherein the antibody or antibody fragment is a conjugated to a cytotoxic agent. 207. The antibody or antibody fragment of 12, wherein the cytotoxic agent is a radioactive isotope or a toxin. 208. The antibody or antibody fragment of one of embodiments 195-207, wherein the antibody or antibody fragment is conjugated to a sequence derived from 4-1 BB or CD28, or a combination thereof. 209. The antibody or antibody fragment of one of embodiments 195-208, wherein the antibody or fragment is produced in HEK293 cells. 210. The antibody or antibody fragment of one of embodiments 195-209, wherein the antibody is a scFv. 211. The antibody or antibody fragment of embodiment 210, wherein the scFv comprises or is the SEQ ID NO: 92, 96, 100, 104, 108, 112, 116, or 120. 212. The antibody or antibody fragment of embodiment 210, wherein the antibody or antibody fragment comprises the SEQ ID NO: 92, 96, 100, 104, 108, 112, 116, or 120. 213. A composition comprising the antibody or fragment of one of embodiments 195-212 and a pharmaceutically acceptable carrier. 214. An article of manufacture comprising a container and a composition contained therein, wherein the composition comprises the antibody or fragment of one of embodiments 195-212. 215. A polynucleotide that encodes the antibody or fragment of one of embodiments 195-212. 216. An expression vector encoding the antibody or fragment of one of embodiments 195-212. 217. A host cell comprising a nucleic acid of any one of embodiments 21 or 216. 218. A method of treating a subject having a UPK2 positive tumor (e.g., urothelial cancer and bladder cancer), comprising administering to the subject a therapeutically effective amount of the antibody or fragment of one of embodiments 195-212. 219. A method of treating a subject having urothelial cancer or bladder cancer, comprising administering to the subject a therapeutically effective amount of the antibody or fragment of one of embodiments 195-212. 220. A chimeric antigen receptor (CAR) comprising an antigen binding domain comprising the antibody or fragment of one of embodiments 195-212 221. A polynucleotide that encodes the CAR of embodiment 220. 222. A modified cell comprising a nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an UPK2 antigen binding domain comprising the antibody or fragment of one of embodiments 195-212. 223. The modified cell of embodiment 222, wherein the CAR further comprises a transmembrane domain, and an intracellular domain and a signaling domain of a co-stimulatory molecule. 224. The modified cell of embodiment 223, wherein the intracellular domain comprising a CD3-zeta signaling domain 225. The modified cell of one of embodiments 222-224, wherein the antigen binding fragment is a scFv. 226. The modified cell of one of embodiments 222-224, wherein the scFv comprises the amino acid sequence of SEQ ID NO: 92. 96, 100, 104, 108, 112, 116, or 120. 227. The modified cell of one of embodiments 222-224, wherein the modified cell comprises a vector that comprises a nucleic acid sequence comprising the SEQ ID NO: 91, 95, 99, 103, 107, 111, 115, or 119. 228. The modified cell of embodiment 227, wherein the vector is a lentiviral vector. 229. The modified cell of one of embodiments 222-228, wherein the modified cell is a T cell derived from a primary human T cell isolated from a patient. 230. The modified cell of one of embodiments 222-228, wherein the modified cell is a T cell derived from a primary human T cell isolated from a human donor. 231. The modified cell of embodiment 229, wherein the cell has a reduced expression of endogenous TRAC gene. 232. The modified cell of one of embodiments 222-231, wherein the modified cell comprises an additional CAR, and the additional CAR binds an antigen of a white blood cell. 233. The modified cell of embodiment 232, wherein the antigen of the white blood cell is a B cell antigen. 234. The modified cell of embodiment 233, wherein the antigen of the B cell antigen is CD19, CD20, CD22, or BCMA. 235. The modified cell of one of embodiments 222-234, wherein the modified cell comprises a dominant negative PD-1. 236. The modified cell one of embodiments 222-234, wherein the modified cell comprises a modified PD-1 lacking a functional PD-1 intracellular domain. 237. The modified cell of one of embodiments 222-234, wherein the intracellular domain comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. 238. The modified cell of embodiment 237, wherein the antigen is Epidermal growth factor receptor (EGFR), Variant III of the epidermal growth factor receptor (EGFRvIII), Human epidermal growth factor receptor 2 (HER2), Mesothelin (MSLN), Prostate-specific membrane antigen (PSMA), Carcinoembryonic antigen (CEA), Disialoganglioside 2 (GD2), Interleukin-13Ra2 (IL13Rα2), Glypican-3 (GPC3), Carbonic anhydrase IX (CAIX), L1 cell adhesion molecule (L1-CAM), Cancer antigen 125 (CA125), Cluster of differentiation 133 (CD133), Fibroblast activation protein (FAP), Cancer/testis antigen 1B (CTAG1B), Mucin 1 (MUC1), Folate receptor-α (FR-α), CD19, FZD10, TSHR, PRLR, Muc 17, GUCY2C, CD207, CD3, CD5, B-Cell Maturation Antigen (BCMA), or CD4. 239. The modified cell of one of embodiment 222-238, wherein the modified cell is a T cell, NK cell, or dendritic cells. 240. The modified cell of one of embodiment 222-239, wherein the modified cell further comprises a nucleic acid sequence encoding a therapeutic agent 241. The modified cell of embodiment 240, wherein the therapeutic agent is present in the modified cell in a recombinant DNA construct, in an mRNA, or in a viral vector. 242. The modified cell of embodiment 240, wherein the modified cell comprises a therapeutic agent mRNA encoding the therapeutic agent, and the mRNA is not integrated into the genome of the modified cell. 243. The modified cell of embodiment 240, wherein the modified cell comprises a nucleic acid sequence comprising or the isolated nucleic acid sequence comprises a promoter comprising a binding site for a transcription modulator that modulates the expression and/or secretion of the therapeutic agent in the cell. 244. The modified cell of embodiment 243, wherein the transcription modulator is or includes Hif1a, NFAT, FOXP3, and/or NFkB. 245. The modified cell of embodiment 243, wherein the promoter is responsive to the transcription modulator. 246. The modified cell of embodiment 243, wherein the promoter is operably linked to the nucleic acid sequence encoding the therapeutic agent such that the promoter drives expression and/or secretion of the therapeutic agent in the cell. 247. A pharmaceutical composition comprising the modified cell of one of embodiments 168-53. 248. A method of eliciting and/or enhancing T cell response in a subject in need thereof and/or treating a tumor of the subject, the method comprising administering an effective amount of the composition of embodiment 247 to the subject. 249. An isolated nucleic acid sequence encoding a binding molecule comprising a first and a second binding domain, wherein the first binding domain binds an antigen, and the second binding domain binds the T cell CD3 receptor complex. 250. The isolated nucleic acid of embodiment 249, wherein the antigen is Epidermal growth factor receptor (EGFR), Variant III of the epidermal growth factor receptor (EGFRvlll), Human epidermal growth factor receptor 2 (HER2), Mesothelin (MSLN), Prostate-specific membrane antigen (PSMA), Carcinoembryonic antigen (CEA), Disialoganglioside 2 (GD2), Interleukin-13Ra2 (IL13Ra2), Glypican-3 (GPC3), Carbonic anhydrase IX (CAIX), L1 cell adhesion molecule (L1-CAM), Cancer antigen 125 (CA125), Cluster of differentiation 133 (CD133), Fibroblast activation protein (FAP), Cancer/testis antigen 1B (CTAG1B), Mucin 1 (MUC1), Folate receptor-α (FR-α), CD19, FZD10, TSHR, PRLR, Muc 17, GUCY2C, CD207, CD3, CD5, B-Cell Maturation Antigen (BCMA), or CD4. 251. The isolated nucleic acid sequence of embodiment 249, wherein the second binding domain binds CD3 epsilon, and/or the first binding domain comprises one of acid sequence of SEQ ID NO: 30, 34, 38, 42, 46, 64, 68, 92, 96, 100, 104, 108, 112, 116, 120, and 136-172. 252. The isolated nucleic acid sequence of embodiment 249, wherein the first binding domain binds tn-Muc1, TSHR, FZD10, PRLR, Muc 16, Muc 17, GUCY2C, CD207, CLDN18.2, CLDN6, or SIGL1C. 253. The isolated nucleic acid sequence of embodiment 249, wherein the isolated nucleic acid sequence encodes a polypeptide comprising one of the amino acid sequences of SEQ ID NO: 123-135. 254. A vector comprising a nucleic acid sequence as defined in any one of embodiments 249-253. 255. A host cell transformed or transfected with the nucleic acid sequence as defined in any one of embodiments 1-5 or with the vector as defined in embodiment 254. 256. A method for the production of a binding molecule according to any one of embodiments 1 to 4, the method comprising culturing a host cell as defined in embodiment 254 under conditions allowing the expression of the binding molecule as defined in any one of embodiments 1 to 4 and recovering the produced binding molecule from the culture. 257. A pharmaceutical composition comprising a binding molecule according to any one of embodiments 1 to 4 or produced according to the method of embodiment 256. 258. A kit comprising a binding molecule as defined in any one of embodiments 1 to 4, a nucleic acid molecule as defined in any one of embodiments 1-4, a vector as defined in embodiment 253, and/or a host cell as defined in embodiment 7. 259. A method for the treatment or amelioration of a disease, comprising administering to a subject in need thereof the binding molecule according to any one of embodiments 1 to 4, or method according to the method of embodiment 256. 260. The method of embodiment 259, further comprising: administering to the subject in need thereof an effective amount of T cell comprising an antigen binding molecule that binds a cell surface molecule of a white cell, wherein the cell surface molecule of the white cell is CD19, CD22, CD20, BCMA, CD5, CD7, CD2, CD16, CD56, CD30, CD14, CD68, CD11b, CD18, CD169, CD1c, CD33, CD38, CD138, or CD13. 261. The method of embodiment 260, wherein the antigen binding molecule comprises the antigen binding domain, a transmembrane domain, a co-stimulatory signaling region, and a CD3 zeta signaling domain. 262. The method of embodiment 261, wherein the T cell has an additional CAR binding the antigen. 263. An isolated nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, the extracellular domain comprising at least two binding domains binding a tumor antigen. 264. The isolated nucleic acid sequence of embodiment 263, wherein the at least two binding domains are scFv binding ta-Muc1 and not ta-Muc1 antigen, respectively. 265. The isolated nucleic acid sequence of embodiment 263, wherein the least two binding domains comprise an antigen binding domain binding ta-Muc1, and an additional antigen biding domain binding an antigen different from ta-Muc1. 266. The isolated nucleic acid sequence of embodiment 265, wherein the antigen different from ta-Muc1 is Epidermal growth factor receptor (EGFR), Variant III of the epidermal growth factor receptor (EGFRvIII), Human epidermal growth factor receptor 2 (HER2), Mesothelin (MSLN), Prostate-specific membrane antigen (PSMA), Carcinoembryonic antigen (CEA), Disialoganglioside 2 (GD2), Interleukin-13Ra2 (IL13Ra2), Glypican-3 (GPC3), Carbonic anhydrase IX (CAIX), L1 cell adhesion molecule (L1-CAM), Cancer antigen 125 (CA125), Cluster of differentiation 133 (CD133), Fibroblast activation protein (FAP), Cancer/testis antigen 1B (CTAG1B), Folate receptor-α (FR-α), CD19, FZD10, TSHR, PRLR, Muc 17, GUCY2C, CD207, CD3, CD5, B-Cell Maturation Antigen (BCMA), or CD4. 267. The isolated nucleic acid sequence of embodiment 263, wherein the intracellular domain comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule selected from the group consisting of CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and any combination thereof. 268. The isolated nucleic acid sequence of embodiment 263, wherein the at least two binding domains comprise SEQ ID NO: 135 and one of SEQ ID NO: 30, 34, 38, 42, 46, 64, 68, 92, 96, 100, 104, 108, 112, 116, 120, and 136-172. 269. The isolated nucleic acid sequence of embodiment 15, wherein the at least two binding domains comprise SEQ ID NO: 70 and one of SEQ ID NO: 59-84. 270. A population of CAR cells comprising the isolated nucleic acid sequence of any one of embodiments 249-253 and 263-268. 271. A pharmaceutical composition comprising the population of the CAR cells of embodiment 270. 272. A method of eliciting and/or enhancing T cell response, eliciting or causing T cell response in a subject in need thereof and/or treating a tumor of the subject, the method comprising administering an effective amount of the composition of embodiment 271 to the subject. 273. One or more modified cells including two or more different antigen binding domains, wherein at least a first antigen binding domain binds a cell surface marker and the second antigen binding domain binds tumor antigen. 274. The one or more modified cells of embodiment 273, wherein the cell surface marker includes the cell surface marker of a white blood cell. 275. The one or more modified cells of embodiment 273 or 274, wherein the tumor antigen includes one or more of SIGLEC15, SLC6A3, KISS1R, QRFPR, GPR119, CLDN6, UPK2, ADAM12, SLC45A3, ACPP, MUC21, MUC16, MS4A12, or ALPP. 276. The one or more modified cells of any one of embodiments 273-275, wherein the antigen binding domains are on the same CAR molecule, different CAR molecules, or on a CAR molecule and a T cell receptor. 277. The one or more modified cells of any one of embodiments 273-276, wherein the two or more different antigen binding domains are on different CAR molecules on different modified cells. 278. The one or more modified cells of any one of embodiments 273-277, wherein the two or more different antigen binding domains are on a CAR molecule and a T cell receptor which are on different modified cells. 279. A population of cells comprising the one or more modified cells of any one of embodiments 273-278. 280. Use of the nucleic acid sequences, the CAR molecules, the antibodies, the vectors, the cells, the population of cells, the compositions, the pharmaceutical compositions, the kit, or the methods of any one of embodiments 1-279 for use in a method of treating a subject's body by therapy. 281. The use of embodiment 280, wherein the subject is a human or animal. 282. The use of embodiment 280 or 281, wherein the subject is suffering from cancer. 283. The use of any one of embodiments 280-282, wherein the use elicits and/or enhances a T cell response in the subject. 284. Use of the nucleic acid sequences, the CAR molecules, the antibodies, the vectors, the cells, the population of cells, the compositions, the pharmaceutical compositions, the kit, or the methods of any one of embodiments 1-279 for use in a method of eliciting and/or enhancing a T cell response in a subject. 285. The use of embodiment 284, wherein the subject is a human or animal. 286. The use of embodiment 284 or 285, wherein the subject is suffering from cancer.

EXAMPLES

The present disclosure is further described by reference to the following examples. These examples are provided for purposes of illustration only and are not intended to be limiting unless otherwise specified. Thus, the present disclosure should in no way be construed as being limited to the following examples, but rather, should be construed to encompass any and all variations which become evident as a result of the teaching provided herein.

Expression of CAR on T Cells

Lentiviral vectors that encode a CAR were generated (see Chimeric Receptors Containing CD137 Signal Transduction Domains Mediate Enhanced Survival of T Cells and Increased Antileukemic Efficacy In Vivo Molecular Therapy vol. 17 no. 8, 1453-1464 August 2009 incorporated herein by reference) and were introduced into human T cells.

Primary T cells were obtained from patients. The obtained primary T cells were transduced with lentiviral vectors to obtain modified T cells. Flow-cytometry was performed and analyzed to confirm the expression of CARs in primary T cells (FIG. 2). Techniques related to cell cultures, construction of lentiviral vectors, and flow cytometry may be found in Control of large, established tumor xenografts with genetically retargeted human T cells containing CD28 and CD137 domains. 3360-3365 PNAS Mar. 3, 2009, vol. 106 no. 9, which is incorporated herein by reference.

Expression of Antigens and Related Tumor Analysis

Detection of mRNA and protein expression levels of target molecules in human cells using experimental methods such as qPCR and FACS were performed. It has been shown that some of the target molecules listed below are specifically expressed in the corresponding tumor cells with relatively low expression or undetectable expression in normal tissue. For example, eight genes were localized in normal tissues and overexpressed in tumor cells. The target point and the corresponding relationship between the tumor are provided in the Table 4. Various assays (e.g., killing) were perform, and results are shown in FIGS. 3-7. Techniques related to cell cultures, construction of cytotoxic T-lymphocyte assay may be found in “Control of large, established tumor xenografts with genetically retargeted human T cells containing CD28 and CD137 domains,” PNAS, Mar. 3, 2009, vol. 106 no. 9, 3360-3365, which is incorporated herein by reference in its entirety.

TABLE 4 Subcellular Organ mainly Target Target SEQ Gene name localization expressing Tumor ID NO. SIGLEC15 Plasma Expression Urothelial 17 membrane in all normal cancer tissues but very low SLC6A3 Plasma Expression Renal 18 membrane in all normal cancer tissues but very low KISS1R Plasma Expression Renal 19 membrane in all normal cancer tissues but very low QRFPR Plasma Expression Renal 20 membrane in all normal cancer: tissues but very low GPR119 Plasma Expression Pancreatic 21 membrane in all normal cancer tissues but very low CLDN6 Plasma Expression Endometrial 22 membrane in all normal cancer/ tissues but Urothelial very low cancer UPK2 Plasma Urethra/ Urothelial  1 membrane bladder cancer (including bladder cancer) ADAM12 Plasma placenta Breast cancer,  2 membrane pancreatic cancer and the like SLC45A3 Plasma prostate Prostate  3 membrane cancer ACPP Plasma prostate Prostate  4 membrane cancer MUC21 Plasma esophagus Esophageal  5 membrane cancer MUC16 Plasma Cervical/ Ovarian  6 membrane Fallopian tube cancer MS4A12 Plasma the large Colorectal  7 membrane intestine cancer ALPP Plasma Placenta/ Endometrial  8 membrane cervix cancer

Identifying Gene Fusion Antigens

Databases (e.g., TCGA) were analyzed to identify gene fusion products and gene fusion antigens. Hundreds of gene fusion products were identified and determined to be associated with cancer. Among these hundreds of gene fusion products, 33 gene fusion antigen groups were further identified based on predetermined criteria. For example, these gene fusion products were found to be expressed in tumor cells, and both fusion proteins of the fusion genes were located in the cytoplasmic membrane. Information of these 33 gene fusion antigen groups are listed in Table 5. Samples corresponding to each row of Table 5 include TCGA-D8-A1XJ-01A-11R-A14M-07, TCGA-E2-A574-01A-11R-A29R-07, TCGA-FU-A3TX-01A-11R-A22U-07, TCGA-CV-7434-01A-11R-2132-07, TCGA-G7-6793-01A-11R-1965-07, TCGA-DB-5277-01A-01R-1470-07, TCGA-KT-A7W1-01A-11R-A34F-07, TCGA-VM-A8CD-01A-11R-A36H-07, TCGA-DD-A3A5-01A-11R-A22L-07, TCGA-DD-AAEA-01A-11R-A41C-07, TCGA-ZS-A9CF-01A-11R-A381B-07, TCGA-44-7670-01A-11R-2066-07, TCGA-55-7281-01A-11R-2039-07, TCGA-62-8394-01A-11R-2326-07, TCGA-78-7143-01A-11R-2039-07, TCGA-78-7146-01A-11R-2039-07, TCGA-46-6025-01A-11R-1820-07, TCGA-85-7710-01A-11R-2125-07, TCGA-O2-A52V-01A-31R-A262-07, TCGA-FB-AAPZ-01A-11R-A41B-07, TCGA-P8-A5KC-01A-11R-A35K-07, TCGA-WB-A81 D-01A-11R-A35L-07, TCGA-EJ-5510-01A-01R-1580-07, TCGA-EJ-A46G-01A-31R-A26U-07, TCGA-ZG-A9L2-01A-31R-A41O-07, TCGA-ZG-A9L2-01A-31R-A41O-07, TCGA-EI-7002-01A-11R-1928-07, TCGA-DX-A1KZ-01A-11R-A24X-07, TCGA-DX-A2J0-01A-11R-A21T-07, TCGA-DX-A3UF-01A-11R-A30C-07, TCGA-DX-AB2V-01A-11R-A41I-07, TCGA-K1-A6RU-01A-11R-A32Q-07, and TCGA-EB-A24D-01A-11R-A18T-07, each representing a barcode in TCGA database. TCGA barcodes, represents the metadata of the participants and their samples in TCGA database.

TABLE 5 Cancer_ Junc- Span- Breakpoint Breakpoint Gene sub- Gene sub- Cancer type Fusion tion ning 1 2 gene1 description location gene2 description2 location3 breast BRCA GNAS-- 23 51 chr20:58895 chr19:44882 GNAS GNAS Plasma NECTI Nectin cell Plasma invasive NECTIN 684:+ 211:+ complex mem- N2 adhesion mem- carcinoma 2 locus brane molecule 2 brane breast BRCA FGFR1-- 9 42 chr8:384573 chr8:396063 FGFR1 Fibroblast Plasma ADAM ADAM Plasma invasive ADAM18 56:− 07:+ growth mem- 18 metallo- mem- carcinoma factor brane peptidase brane receptor 1 domain 18 cervical CESC WHRN-- 1000 1000 chr9:114403 chr9:115035 WHRN Whirlin Cyto- TNC Tenascin C Extra- squamous TNC 306:− 229:− plasm; cellular; cell Plasma Plasma carcinoma mem- mem- and brane brane endocervical adeno- carcinoma head and HNSC PQLC1-- 28 210 chr18:79943 chr18:79966 PQLC1 PQ loop Plasma HSBP Heat Plasma neck HSBP1L 329:− 612:+ repeat mem- 1L1 shock mem- squamous 1 containing brane factor brane cell 1 binding carcinoma protein 1 like 1 kidney renal KIRP FNDC3B-- 91 307 chr3:172133 chr3:165786 FNDC3 Fibro- Plasma BCHE Butyryl- Plasma papillary cell BCHE 546:+ 311:− B nectin mem- cholin mem- carcinoma type III brane esterase brane domain containing 3B brain lower LGG GRIA4-- 28 113 chr11:10586 chr11:90173 GRIA4 Glutamate Plasma NAAL N-acetylated Plasma grade NAALAD 2208:+ 824:+ ionotropic mem- AD2 alpha-linked mem- glioma 2 receptor brane acidic brane AMPA dipeptidase type 2 subunit 4 brain lower LGG EPHB2-- 6 29 chr1:227850 chrX: 15380 EPHB2 EPH Plasma PDZD PDZ domain Cyto- grade PDZD4 76:+ 8595:− receptor mem- 4 containing 4 plasm; glioma B2 brane Plasma mem- brane brain lower LGG SEC24A-- 11 140 chr5:134649 chr11:65593 SEC24A SEC24 Plasma KCNK Potassium Plasma grade KCNK7 173:+ 874:− homolog mem- 7 two pore mem- glioma A, brane domain brane COPII channel coat subfamily K complex member 7 com- ponent liver LIHC ACVR1B-- 6 43 chr12:51951 chr12:51912 ACVR1 Activin A Plasma ACVR Activin A Plasma hepato- ACVRL1 834:+ 470:+ B receptor mem- L1 receptor like mem- cellular type 1B brane type 1 brane carcinoma liver LIHC ABCC2-- 192 315 chr10:99784 chr10:65920 ABCC2 ATP Plasma CTNN Catenin Cyto- hepato- CTNNA3 781:+ 617:− binding mem- A3 alpha 3 plasm; cellular cassette brane Cyto- carcinoma subfamily ske- C leton; member 2 Plasma mem- brane liver LIHC EFNA1-- 5 17 chr1:155131 chr1:155062 EFNA1 Ephrin A1 Extracel ADAM ADAM Plasma hepato- ADAM15 634:+ 460:+ lular; 15 metall- mem- cellular Plasma opeptidase brane carcinoma mem- domain brane 15 lung LUAD CPNE8-- 16 74 chr12:38905 chr3:858020 CPNE8 Copine 8 Plasma CADM Cell adhesion Plasma adeno- CADM2 437:− 47:+ mem- 2 molecule 2 mem- carcinoma brane brane lung LUAD NOTCH 1000 1000 chr1:119935 chr1:119894 NOTCH Notch 2 Plasma ADAM ADAM Plasma adeno- 2-- 472:− 596:− 2 mem- 30 metallopepti- mem- carcinoma ADAM30 brane dase domain brane 30 lung LUAD CELSR1-- 81 308 chr22:46463 chr1:263201 CELSR Cadherin Plasma CD52 CD52 Plasma adeno- CD52 707:− 71:+ 1 EGF LAG mem- molecule mem- carcinoma seven-pass brane brane G-type receptor 1 lung LUAD ILVBL-- 27 67 chr19:15122 chr19:14950 ILVBL IIvB Plasma SLC1 Solute carrier Plasma adeno- SLC1A6 693:− 390:− aceto- mem- A6 family 1 mem- carcinoma lactate brane member 6 brane synthase like lung LUAD F11R-- 29 220 chr1:161021 chr1:162355 F11R F11 Plasma NOS1 Nitric oxide Cyto- adeno- NOS1A 010:− 187:+ receptor mem- AP synthase 1 plasm; carcinoma P brane adaptor Plasma protein mem- brane lung LUSC CELSR1-- 137 521 chr22:46533 chr22:26292 CELSR Cadherin Plasma SEZ6 Seizure Plasma squamous SEZ6L 627:− 406:+ 1 EGF LAG mem- L related 6 mem- cell seven-pass brane homolog like brane carcinoma G-type receptor 1 lung LUSC KIRREL-- 10 64 chr1:157993 chr1:158255 KIRREL Kin of Plasma CD1A CD1a Endo- squamous CD1A 728:+ 084:+ IRRE mem- molecule some; cell like brane Golgi carcinoma (Dro- appa- sophila) ratus; Plasma mem- brane lung LUSC ATP10D-- 20 79 chr4:475256 chr4:462506 ATP10D ATPase Plasma GABR Gamma- Plasma squamous GABRA 42:+ 04:− phos- mem- A2 aminobutyric mem- cell 2 pholipid brane acid type A brane carcinoma trans- receptor porting alpha2 10D subunit (putative) pancreatic PAAD ORAI2-- 7 17 chr7:102439 chr17:19681 ORAI2 ORAI Plasma SLC4 Solute carrier Plasma adeno- SLC47A 181:+ 670:− calcium mem- 7A2 family 47 mem- carcinoma 2 release- brane member 2 brane activated calcium modulator 2 pheochromo- PCPG ADCYA 5 25 chr7:311002 chr7:309749 ADCYA ADCYAP Plasma GHRH Growth Plasma cytoma and P1R1-- 10:+ 71:+ P1R1 receptor mem- R hormone mem- para- GHRHR type I brane releasing brane ganglioma hormone receptor pheochromo- PCPG TMEM1 15 107 chr7:141212 chr7:154769 TMEM1 Trans- Plasma DPP6 Dipeptidyl Plasma cytoma and 78B-- 704:+ 417:+ 78B mem- mem- peptidase mem- para- DPP6 brane brane like 6 brane ganglioma protein 178B prostate PRAD ADAM9-- 5 28 chr8:389971 chr8:538792 ADAM9 ADAM Plasma RGS2 Regulator of Plasma adeno- RGS20 60:+ 58:+ metallo- mem- 0 G-protein mem- carcinoma peptidase brane signaling 20 brane domain 9 prostate PRAD FAM 160 10 35 chr10:11483 chr10:11266 FAM160 Family Plasma VTI1A Vesicle Plasma adeno- B1-- 6246:+ 8218:+ B1 with mem- transport mem- carcinoma VTI1A sequence brane through brane similarity interaction 160 with t- member SNAREs 1A B1 prostate PRAD TMPRS 22 56 chr21:41494 chr21:42743 TMPRS Trans- Plasma PDE9 Phosphodiest Plasma adeno- S2-- 356:− 776:+ S2 membrane mem- A erase 9A mem- carcinoma PDE9A protease, brane brane serine 2 prostate PRAD PDE9A-- 17 40 chr21:42733 chr21:41498 PDE9A Phospho- Plasma TMPR Trans- Plasma adeno- TMPRS 426:+ 189:− diesterase mem- SS2 membrane mem- carcinoma S2 9A brane protease, brane serine 2 rectum READ LHFPL2-- 8 62 chr5:785097 chr6:128089 LHFPL2 Lipoma Plasma PTPR Protein Plasma adeno- PTPRK 84:− 992:− HMGIC mem- K tyrosine mem- carcinoma fusion brane phosphatase, brane partner- receptor type like 2 K sarcoma SARC TM7SF3-- 13 82 chr12:26990 chr12:75051 TM7SF3 Trans- Plasma KCNC Potassium Plasma KCNC2 450:− 317:− membrane mem- 2 voltage-gated mem- 7 brane channel brane super- subfamily C family member 2 member 3 sarcoma SARC MPZL1-- 16 175 chr1:167776 chr1:173188 MPZL1 Myelin Plasma TNFS Tumor Plasma TNFSF4 166:+ 569:− protein mem- F4 necrosis mem- zero brane factor brane like 1 superfamily member 4 sarcoma SARC GNG7-- 5 6 chr19:25206 chr15:69399 GNG7 G protein Plasma PAQR Progestin Plasma PAQR5 08:− 974:+ subunit mem- 5 and adipoQ mem- gamma 7 brane receptor brane family member 5 sarcoma SARC KIRREL-- 1000 1000 chr1:157993 chr1:158256 KIRREL Kin of Plasma CD1A CD1a Endo- CD1A 728:+ 786:+ IRRE mem- molecule some; like brane Golgi (Dro- appa- sophila) ratus; Plasma mem- brane sarcoma SARC P2RX5-- 28 103 chr17:36795 chr17:35722 P2RX5 Purinergic Plasma TRPV Transient Plasma TRPV1 90:− 49:− receptor mem- 1 receptor mem- P2X5 brane potential brane cation channel subfamily V member 1 skin SKCM PTPRG-- 6 55 chr3:617489 chr3:634808 PTPRG Protein Plasma SYNP Synap- Plasma cutaneous SYNPR 82:+ 32:+ tyrosine mem- R toporin mem- melanoma phos- brane brane phatase, receptor type G

TABLE 6 Identifier and related Sequences SEQ SEQ SEQ ID ID ID Identifier NO: Identifier NO: Identifier NO: UPK2 1 Hinge 25 VL1 VH1 SIGLEC-15- 49 CAR-2 ADAM 12 2 TM 26 VL1 VH2 SIGLEC-15- 50 CAR-3 SLC45A3 3 4-1BB 27 VL1 VH3 SIGLEC-15- 51 CAR-4 ACPP 4 CD3 zeta 28 VL1 VH 4 SIGLEC-15- 52 CAR-5 MUC21 5 CLDN6-CAR-1 29 VL2 VH 1 SIGLEC-15- 53 CAR-6 MUC16 6 ScFv CLDN6- 30 VL2 VH2 SIGLEC-15- 54 CAR-1 CAR-7 MS4A12 7 ScFv VL CLDN6- 31 VL2 VH3 SIGLEC-15- 55 CAR-1 CAR-8 ALPP 8 ScFv VH CLDN6- 32 VL2 VH4 SIGLEC-15- 56 CAR-1 CAR-9 SLC2A14 9 CLDN6-CAR-2 33 VL1 SIGLEC-15-CAR 57 GS1-259H13.2 10 ScFv CLDN6- 34 VL2 SIGLEC-15-CAR 58 CAR-2 ERVFRD-1 11 ScFv VL CLDN6- 35 VH1 SIGLEC-15-CAR 59 CAR-2 ADGRG2 12 ScFv VH CLDN6- 36 VH2 SIGLEC-15-CAR 60 CAR-2 ECEL1 13 CLDN6-CAR-3 37 VH3 SIGLEC-15-CAR 61 CHRNA2 14 scFv CLDN6-CAR- 38 VH4 SIGLEC-15-CAR 62 3 GP2 15 scFv VL CLDN6- 39 MUC16-CAR-1 63 CAR-3 PSG9 16 scFv VH CLDN6- 40 scFv MUC16-CAR-1 64 CAR-3 SIGLEC15 17 CLDN6-CAR-4 41 scFv VLMUC16-CAR-1 65 SLC6A3 18 scFv CLDN6-CAR- 42 scFv VH MUC16-CAR- 66 4 1 KISS1R 19 scFv VL CLDN6- 43 MUC16-CAR-2 67 CAR-4 QRFPR 20 scFv VH CLDN6- 44 scFv MUC16-CAR-2 68 CAR-4 GPR119 21 SIGLEC-15-CAR-1 45 scFv VL MUC16-CAR-2 69 CLDN6 22 scFv SIGLEC-15- 46 scFv VH MUC16- 70 CAR-1 CAR-2 SP 23 scFv VL SIGLEC- 47 KISS1R-CAR 71 15-CAR-1 Linker 24 scFv VH SIGLEC- 48 Ligent peptide  72 15-CAR-1 KISS1R-CAR 6503 S5D1 VL NA 73 6503 S5D1 VL aa 82 scFv UPK2-S3D10 NA 107 6503 S5D1 VH 74 6503 S5D1 VH aa 83 scFv UPK2-S3D10 aa 108 NA 6504 S5F2 VL NA 75 6504 S5F2 VL aa 84 VLUPK2-S3D10 aa 109 6504 S5F2 VH NA 76 6504 S5F2 VH aa 85 VH UPK2-S3D10 aa 110 6502 S12E9 VL 77 6502 S12E9 VL aa 86 scFv UPK2-S7F9 NA 111 NA 6502 S12E9 VH 78 6502 S12E9 VH aa 87 scFv UPK2-S7F9 aa 112 NA 6501 S10E12 VL 79 6501 S10E12 VL 88 VL UPK2-S7F9 aa 113 NA aa 6501 S10E12 VH 80 6501 S10E12 VH 89 VH UPK2-S7F9 aa 114 NA aa 3xGGGGS NA 81 3xGGGGS aa 90 scFv UPK2-S7F11 NA 115 scFv UPK2-S2B7 91 scFv UPK2-S3A4 99 scFv UPK2-S7F11 aa 116 NA NA scFv UPK2-S2B7 92 scFv UPK2-S3A4 100 VL UPK2-S7F11 aa 117 aa AA VH UPK2-S2B7 93 VL UPK2-S3A4 AA 101 VH UPK2-S7F11 aa 118 aa VL UPK2-S2B7 94 VH UPK2-S3A4 AA 102 scFv UPK2-S7F11 NA 119 aa scFv UPK2-S2E2 95 scFv UPK2-S3C10 103 scFv UPK2-S7F11 aa 120 NA NA scFv UPK2-S2E2 96 scFv UPK2-S3C10 104 VL UPK2-S7F11 aa 121 aa AA VL UPK2-S2E2 97 VL UPK2-S3C10 105 VH UPK2-S7F11 aa 122 aa AA VH UPK2-S2E2 98 VH UPK2-S3C10 106 MUC1-1 HL CD3 HL 123 aa AA MUC1-2 HL CD3 124 FZD10 HL CD3 HL 125 TSHR HL CD3 HL 126 HL PRLR HL CD3 HL 127 MUC17 HL CD3 128 GUCY2C HL CD3 HL 129 HL CD207 HL CD3 130 CLDN18.2 HL CD3 131 CLDN6 HL CD3HL 132 HL HL SIGL1C-15 HL 133 muc16 HL cd3 HL 134 Cd3 HL 135 CD3 HL scFv TSHR 136 scFv PRLR 137 scFv Muc 17 138 scFv GUCY2C 139 scFv 140 Prolactin 141 CD207 (ligand) scFv CD3 142 scFv CD4 143 scFv CD4-2 144 scFv CD5 145 scfv CD33 146 scfv CD123 147 scfv ROR1 148 scfv CD70 149 scfv CD 133 150 scfv GPC3 151 scfv EpCAM 152 scfv CD20 153 scfv CD22 154 scfv CD30 155 scfv CD5 156 scfv Her2 157 scfv CEA 158 scfv PSCA 159 scfv TAG-72 160 scfv CD38 161 scfv EGFRV III 162 scfv EphA2 163 scfv FAP 164 scfv GD2 165 scfv GD3 166 scfv IL13R-2a 167 scfv NKG2D 168 scfv PSMA 169 scfv survivin 170 Tumor 171 associated MUC1 scFv scfv 172 scFv 6503 173 scFv 6504 S5F2 174 Mesothelin S5D1 scFv 6502 175 scFv 6501 176 scFv S4C7 177 S12E9 S10E12 scFv S12D4 178 scFv S9F5 179 6502 S12E9 VL 180 6502 S12E9 VH 181 S4C7VH 182 S4C7VL 183 S12D4VH 184 S12D4VL 185 S9F5VH 186 S9F5VL 187 4xGGGGS 188 PmCGR 189 PmCKR 190 scFv: Signal peptide + VL + 3xGGGGS + VH

Anti-SINGLEC-15 CAR and Anti-KISSR CAR

FIG. 2 shows flow cytometry analysis of T cells expressing CARs. On Day 1, CD3 positive T cells were sorted. On Day 3, the T cells were infected with lentivirus encoding CAR (multiplicity of infection (MOI): 50:1), On Day 5-6, expression assay was performed. On Day 6, T cells were cultured with 3T3-antigen-mcherry-SC with ratio 30:1. Sequences and corresponding references listed in FIGS. 2-7 are listed in Table 7.

FIG. 3 shows results of a killing assay of anti-SIGLEC15 CAR (SIGLEC15-CAR SEQ ID NO: 46, 50, 51, and 52). It was observed that anti-SIGLEC15 CAR T cells killed the substrate cells. The negative control SIGLEC15 alone group was the group without the added anti-SIGLEC 15 CAR T cells, and the NT group was added to non-transfected T cells. FIGS. 4 and 5 show results of cytokine release assays of anti-SIGLEC15 CAR cocultured with the substrate cells.

TABLE 7 Target Seq ID ID SIGLEC 15 49 CAR6  51 CAR8  52 CAR9  53 CAR10 46 CAR5  50 CAR7  54 CAR11 55 CAR12 56 CAR13 Klss1R 71 CAR14

FIG. 6 shows results of a killing assay of anti-KISSR CAR (KISSR-CAR: SEQ ID NO: 71). It was observed that anti-KISS1R CAR T cells killed the substrate cells. The NT group was added to non-transfected T cells. FIG. 7 show results of cytokine release assays of anti-KISSR CAR T cells co-cultured with the substrate cells.

ACPP Antibody Preparation and Anti-ACPP CAR

FIGS. 8-10 show flow cytometry assay for ACPP antibodies. 293T cells were transfected with the pcDNA-ACPP-flag plasmid to express the C-terminal flag-tagged ACPP protein. After 2 days, staining was detected using 7 ACPP antibodies and flag tag antibody staining. ACPP single staining does not break the membrane staining, first add ACPP primary antibody, then use goat anti human-FITC secondary antibody. When the flag label is single-dyed, APC direct-labeled primary antibody is used and the membrane is stained. Flag/ACPP double staining when ruptured. The Flag tag antibody detected 26.39% of the cells expressing the antigen. The S5D1 antibody detected 30.35% of cells expressing ACPP antigen. The double staining results showed that the positive cells had the same ACPP and flag expression levels. The staining results are specific. S5F2 also has a weaker binding, and the rest of the antibody flow has no signal. The transfected plasmid was able to express a C-terminal flag-tagged ACPP transmembrane protein on 293T cells. Flow cytometry experiments demonstrated that ACPP antibody S5D1 has good binding ability to antigen expressed on cell membrane. Flag labeling confirmed the normal expression of the protein.

For the affinity assay in FIG. 10, the affinity of two monoclonal antibodies, S5D1 and S5F2, was analyzed using GE's BIAcore X-100 Biomolecular Interaction Analyzer. Affinity analysis was performed using a conventional procedure. The human monoclonal antibody S5D1 or S5F2 was captured using an anti-human antibody coated on a chip. Affinity analysis was then performed using different concentrations of recombinantly expressed PAP as the mobile phase. The affinity of the monoclonal antibody S5D1 is about 9 nM. It is speculated that the affinity of S5F2 is lower than 100 nM. S5D1 has a higher affinity for ACPP antigen. The sequences of the antibodies are listed in Table 6.

The ACPP antibodies were generated by cloning and expressing the selected serum prostatic acid phosphatase (PAP) antigen and screening using the prepared PAP antigen of the phage display human antibody library (humanphagedisplay). The ACPP gene sequence was cloned into the recombinant antigen expression vector PTSE-His. The constructed recombinant plasmid was transfected into HEK293 cells. The recombinant protein was purified using GE's Histrap FF affinity chromatography column. The human single-chain antibody library was screened using ACPP-His as an antigen with reference to a classical solid-phase screening strategy. The single-chain antibody library consists of a total of 12 sub-libraries of fully synthetic human single-chain antibody, natural human single-chain antibody and semi-synthetic-semi-natural single-chain antibody library. The total library capacity exceeds 10E9, and the correct rate is about 75%. Three rounds of routine screening were performed using solid phase coated antigens. After the second round of screening and after the third round of screening, 600 monoclonal clones (1200 monoclonal clones) were randomly selected for monoclonal identification. Approximately 40 positive monoclonal capable of specifically binding to PAP were obtained. Sequence analysis was performed on all monoclonal. The results showed that these positive clones shared 7 different antibody sequences. Representative clones are S4C7, S5D1, S5F2, S9F5, S10E12, S12D4 and S12D9, respectively (Sequences are listed in Table 6). The genes of the heavy and light chain variable region of the above seven scFvs were cloned into the eukaryotic expression vectors pTSEG1n and pTSEK, respectively. Seven human full antibodies were prepared using the HEK293 cell transient expression system. The recombinantly expressed whole antibody was purified using a Protein A affinity chromatography column.

FIG. 11 shows immunofluorescence staining of paraffin sections of prostate cancer. The corresponding method includes: 1. tissue dehydration; 2. tissue transparency; 3. dipping wax; 4. embedding; 5. slicing and baking the slices; 6. sectioning and dewaxing; 7. antigen retrieval; 8. serum blocking; 9. adding primary antibody; 10. adding fluorescent secondary antibody; 11. serum blocking protecting from light; 12. adding primary antibody; 13. adding fluorescent secondary antibody; 14. complex dye core; and 15. collecting image. As shown, prostate cancer in situ and tissues adjacent to carcinoma in situ have higher ACPP expression. At the same time, the ACPP antibody used for the staining was S5D1, indicating that the antibody can specifically recognize ACPP. S5D1 was selected for further experiments below. The expression of ACPP in tumor tissue sections can be visualized by immunofluorescence staining, and it can also reflect the specificity and sensitivity of the antibody.

FIG. 12 shows 293T cells expressing ACPP. On day 0, the 293T-WT cells were digested and placed on a 6-well plate. On day 1, the cells were infected with the ACPP-lentivirus expression vector. On day 2, the medium was changed to remove the lentivirus, and fresh medium was added. The cells were digested and analyzed by flow cytometry. The antibody for flow cytometry was S5D1 and the antibody usage was 1 ug/100 ul. The flow results showed that the ACPP expression of 293T-ACPP cells was 97.80%. It can be used as an ACPP positive cell in subsequent experiments. ACPP can be overexpressed in 293T cells as an ACPP positive cell for experiments to assess the function of ACPP CAR T cells.

FIG. 13 shows flow cytometry assay of T cells expressing anti-ACPP CAR (anti-ACPP scFv: SEQ ID: 173). On day 0, peripheral blood from healthy volunteers was drawn; CD3+ T cells were sorted; and CD3/CD28 Dynabeads were added at a 1:1 ratio. On Day 1, T cells were transduced with vectors. CD19CAR T cells were obtained according to the infection ratio of MOI=13; ACPP CAR T cells were obtained according to the infection ratio of MOI=130. On day 2, culturing media were changed, and lentivirus was removed. The cells were then resuspended using fresh medium.

On day 6, flow cytometry was used to detect CAR expression. Since both CD19CAR and ACPP CAR include humanized antibodies, human CAR antibodies are used for detection. As a result, the expression of CD19 CAR in infected T cells was 59.55%, and the expression of ACPP CAR in infected T cells was 26.16%. Since both CD19CAR and ACPP CAR are humanized antibodies, the CAR expression was measured by using human CAR antibody for flow detection.

FIG. 14 shows results of co-culturing assay. The CAR ratio of ACPP CAR T cells and CD19CAR T cells was normalized with NT cells. 10⁴ CAR+ cells and 10⁴ 293T-WT or 293T-ACPP or Nalm-6 cells were co-cultured. CD137 expression of CAR positive CD8 positive cells was detected by flow cytometry after 48 hrs. The left column is the CD137 expression of CAR T cells co-cultured with 293T-WT cells, and the CD137 expression is absent in both the CD19CAR group and the ACPP CAR group. This indicates that CAR T cells cannot be activated due to the absence of specific antigen expression in 293T. In the middle column, CAR T cells were co-cultured with 293T or 293T-ACPP cells overexpressing ACPP. The expression of CD137 in the ACPP CAR group was 27.15%, and that CD137 was not expressed in the CD19CAR group. This indicates that ACPP-CAR T Cells recognized and were activated by ACPP. The right column is a co-culture of CAR T cells with Nalm-6 cells, which are CD19-positive cells that are specifically recognized and activated by CD19CAR T cells. The results showed that the expression of CD137 in the CD19CAR group was 21.01%, and that CD137 was not expressed in the ACPP CAR group. The results are in line with expectations. Taken together, it was demonstrated that ACPP CAR T cells specifically recognize and can be activated by the ACPP antigen. CD137 is a marker protein for the activation of T cells, so the level of CD137 up-regulation of CAR T cells after co-culture with CAR T cells and substrate target cells can be used to determine whether CAR T cells are activated.

FIG. 15 shows IFN-γ release by ACPP CAR T cells in response to ACPP. The CAR ratio of ACPP CAR T cells and CD19 CAR T cells was normalized with NT cells. The experiment was carried out by co-culturing 0.2 or 10⁴ CAR+ cells and 10⁴ 293T-WT or 293T-ACPP or Nalm-6 cells. After 24 hr, the supernatant was collected and the amount of IFN-γ released was examined. Nalm-6 is a CD19 positive cell, and 293T-ACPP is a 293T cell overexpressing ACPP. FIG. 15 is a graph showing the results of CAR T cells: substrate cells of 1:1. ACPP CAR T cells exhibit significant IFN-γ release when co-cultured with 293T-ACPP, indicating that 293T-ACPP can be recognized by ACPP CAR T cells and release IFN-γ to kill target cells. At the same time, Nalm-6 can also be recognized by CD19CAR T cells and release IFN-γ to kill target cells. Furthermore, Nalm-6 did not stimulate the release of IFN-γ by ACPP CAR T cells. CD19 CAR T cells were also unable to stimulate IFN-γ release by 293T-ACPP. In sum, ACPP CAR T cells can specifically recognize ACPP-positive target cells and release IFN-γ to kill target cells under their stimulation. During the process of killing target cells by T cells, a large amount of cytokines such as IFN-γ are usually released to enhance the killing ability. Therefore, whether the CAR T cell has the ability to kill the target cell can be determined by the amount of IFN-γ released when the CAR T cell is co-cultured with the substrate target cell.

FIG. 16 shows that CAR expression of ACPP CAR on T cells can be measured by detecting human CAR antibody. On day 0, peripheral blood from healthy volunteers was drawn; CD3+ T cells were sorted; and CD3/CD28 Dynabeads were added in a 1:1 ratio. On Day 1, T cells were transduced with vectors. CD19CAR T cells were obtained according to the infection ratio of MOI=1; ACPP CAR T cells were obtained according to the infection ratio of MOI=50. On day 2, culturing media were changed and lentivirus was removed. The cells were then resuspended using fresh medium. On day 6, flow cytometry was used to detect CAR expression. Since both CD19CAR and ACPP CAR are humanized antibodies, human CAR antibodies are used for detection. The results are shown in the figure. The expression of CD19CAR in CD19CAR T cells was 50.64%, and the expression of ACPP in ACPP CAR T cells (6501) was 37.2%, in ACPP CAR T cells (6503) was 33.93%, and in ACPP CAR T cells (6504) was 45.63%. Since both 19CAR and ACPP CAR are humanized antibodies, the CAR expression level can be obtained by using human CAR antibody for flow detection.

FIG. 17 shows cytokine release by ACPP CAR T cells in response to ACPP. The CAR ratio of ACPP CAR T cells and CD19 CAR T cells was normalized with NT cells. The experiment was carried out with 0.2 or 1×10⁴CAR+ cells co-cultured with 1×10⁴ 293T-ACPP or Nalm-6 cells, and the supernatant was collected after 24 hrs to detect IFN-γ and IL2. Nalm-6 is a CD19 positive cell, and 293T-ACPP is a 293T cell overexpressing ACPP. FIG. 17 shows that ACPP CAR T 6503 exhibits significant increased release of IFN-γ and IL2 when co-cultured with 293T-ACPP, indicating that ACPP CAR T 6503 cells recognize 293T-ACPP and activate the release of IFN-γ and IL2. In contrast, ACPP CAR T 6501 and 6504 cells could not activate the release of IFN-γ and IL2. At the same time, CD19CAR T cells were able to recognize Nalm-6 and activate the release of IFN-γ and IL2. Furthermore, Nalm-6 failed to activate ACPP CAR T cells to release IFN-γ. At the same time, CD19CAR T cells could not be activated by 293T-ACPP to release IFN-γ. This indicates that the two targeted CAR T cells are specific. During the process of killing the target cells by T cells, a large amount of cytokines such as IFN-γ and IL2 are usually released to enhance the killing ability. Therefore, whether the CAR T cells have a killing ability against the target cells can be determined by the release amount of IFN-γ and IL2 when the CAR T cells are co-cultured with the substrate target cells.

FIGS. 18 and 19 show CD137 expression in various conditions. CAR 1204 is a human-derived CD19CAR, which can be labeled with human CAR antibody and CD137 antibody. The CAR ratio of ACPP CAR T cells and CD19CAR T cells was normalized with NT cells. 10⁴ CAR+ cells were co-cultured with 10⁴ 293T-ACPP or Nalm-6 cells, and CD137 expression of CD8 positive cells was detected by flow cytometry after 24 hrs. The first row is the result of co-culture of CAR T cells and 293T-ACPP. CD19CAR T cells were not activated by 293T-ACPP to express CD137. ACPP CAR T 6503 cells were activated by 293T-ACPP to express CD137. ACPP CART 6501 and 6504 cells were not activated by 293T-ACPP to express CD137. The second row is the result of co-culture of CAR T cells and the CD19 positive cell line Nalm6. CD19CAR T cells can be activated by Nalm6 to express CD137. All ACPP CAR T cells could not be activated by Nalm6 to express CD137, indicating that CD19CAR T and ACPP CAR T cells are specific. CD137 is a marker protein for the activation of T cells. Thus, it is determined that CAR T cells are activated by detecting the expression of CD137 in CAR T cells after co-culture of CAR T cells and substrate target cells.

UPK2 Antibody Preparation

The recombinant UPK2 extracellular domain (UPK2-His) was prepared using E. coli expression system. BALB/c mice of 6-8 weeks old were taken, and the mice were subjected to tail vein blood sampling to leave the background serum before immunization. The UPK2-His recombinant antigen was immunized for the first time and emulsified with complete Freund's adjuvant. Each mouse was intraperitoneally injected with 50 μg of recombinant antigen. The immunization was boosted at intervals of two weeks, and UPK2-His recombinant antigen was emulsified by incomplete adjuvant. Each mouse was intraperitoneally injected with 50 μg of recombinant antigen for three booster immunizations. The tail vein blood collection was performed before the third booster immunization to analyze the serum UPK2 antibody titer. The results showed that the antibody titer of UPK2 in the serum of three of the four mice reached 10⁶ or more (FIG. 20), indicating that the immunization was successful.

The fifth immunization was changed to shock the immunization, and the UPK2-His recombinant antigen without adjuvant was used as the immunogen. Each mouse was intraperitoneally injected with 50 μg of recombinant antigen, and the mice were sacrificed 3 days after the immunization. Spleen cells were collected from mice and labeled as “left front” in the graph shown in FIG. 20.

The mouse spleen lymphocytes were separated using mouse lymphocyte separation solution (Dakko, CAT #DKW33-R0100), and the isolated lymphocytes were totaled using the total RNA extraction kit (Tiangen, CAT #DP430). RNA extraction. Using the extracted total RNA as a template, the first strand cDNA synthesis kit (Thermo scientific, CAT #K1621) was used to synthesize the heavy chain variable region and the light chain variable region, respectively. The reverse transcription primers were gene-specific primers, and the primer pairing was performed. The regions are located in the antibody heavy chain constant region and the antibody light chain constant region, respectively, and the specific sequences are PmCGR: TGCATTTGAACTCCTTGCC (SEQ ID NO: 189) and PmCKR: CCATCAATCTTCCACTTGAC (SEQ ID NO: 190), respectively. The synthesized cDNA was immediately stored at −70° C. for storage. Then, the cDNA was obtained by reverse transcription and used as a template to obtain the primers (Journal of Immunological Methods, 201 (1997), 35-55), and the murine antibodies VH and VK were amplified by PCR, respectively. The overlap extension PCR technique was used to construct a single chain antibody (scFv). Finally, the prepared mouse single-chain antibody gene was cloned into the vector pADSCFV-S to construct a ScFv library. The library capacity of this antibody library reached 1.6×10⁸, and the correct rate was 41.5%.

Using recombinant UPK2-his as the antigen, the mouse single-chain antibody library was screened by reference to the classical solid-phase screening strategy, and three rounds of screening were performed by means of binding, elution, neutralization, infection and amplification, in the second round. After the third round of screening, about 700 monoclonal clones were identified by phage ELISA. Sixty clones with high positive ELISA signal were selected for sequence analysis to obtain eight strains with different sequences that bind to UPK2-His. The eight antibodies are: clone S2B7, S2E2, S3A4, S3C10, S3D10, S7F9, S7F11 and S7G7 (FIG. 21). The heavy and light chain variable region sequences (scFv) of the eight monoclonal antibodies are shown in Table 6.

The heavy and light chain variable region genes of the above eight scFvs were cloned into the eukaryotic expression vectors pTSEG1n and pTSEK, respectively, and eight murine-human chimeric antibodies (murine antibody variable regions) were prepared using the company's HEK293 cell transient expression system. Human antibody constant region). The recombinant whole antibody was purified by Protein A affinity chromatography column, and SDS-PAGE showed. These eight antibodies were normally expressed, and their purity met the level for protein identification.

The ability of recombinant whole antibodies to bind antigen UPK2-His was analyzed using a classical ELISA method. The results are shown in FIG. 22. As shown in FIG. 22, all 8 antibodies can bind to the antigen UPK2-His.

At the same time, the specificity of the prepared monoclonal antibody was analyzed by a similar ELISA method. As shown in FIG. 23, the eight recombinant antibodies can specifically recognize the recombinant UPK2-His, and there are no obvious non-specific bindings of various unrelated antigens.

The affinity of the eight monoclonal antibodies was analyzed using GE's BIAcore X-100. Affinity analysis was performed using a conventional procedure by first capturing the human monoclonal antibody with an anti-human antibody coated on a chip, and then using different concentrations of recombinant UPK2-His as the mobile phase for affinity analysis. As shown in Table 8, the affinity (KD) of these recombinant antibodies is mostly between 0.1 nM and 10 nM. Among them, the binding and dissociation of S7F11/S7G7 were slow, and the binding of S3D10 was too slow. When the three monoclonal antibodies were analyzed by BIAcore X-100 for affinity analysis, the automatic fitting of KD was poor, and the data was for reference only.

TABLE 8 Recombinant anti-UPK2 monoclonal antibody affinity parameters determined by BIAcore Monoclonal antibody Kon Koff KD Remarks S2B7 1.493 × 10⁵ 3.495 × 10⁻³ 2.34 × 10⁸ S3A4 1.125 × 10⁵  3.05 × 10⁻³ 2.712 × 10⁻⁸ S7F9  1.4 × 10⁵ 2.344 × 10⁻³ 1.674 × 10⁻⁸ S2E2 1.381 × 10⁶ 3.894 × 10⁻³  2.82 × 10⁻⁹ S3C10 1.226 × 10⁶ 1.117 × 10⁻³  9.109 × 10⁻¹⁰ S7F11 3.504 × 10³ 8.126 × 10⁻⁶ 2.319 × 10⁻⁹ Kd overrun S7G7 5.049 × 10⁴ 1.202 × 10⁻⁶  2.381 × 10⁻¹¹ Kd overrun S3D10 6.431 × 10² 2.614 × 10⁻³ 4.064 × 10⁻⁶ U-value = 15

In this study, the recombinant UPK2 extracellular domain (UPK2-His) was used to complete the immunization of mice, the construction, screening and monoclonal identification of the murine immune library. Eight murine monoclonal antibodies (S2B7, S2E2, S3A4, S3C10, S3D10, S7F9, S7F11 and S7G7), with different sequences and capable of binding recombinant UPK2 were obtained. and preliminary specificity analysis showed that these monoclonal antibodies specifically bind to recombinant UPK2-his. Affinity analysis based on BIAcore showed that the affinity of these recombinant anti-UPK2 antibodies was mostly between 0.1 nM and 10 nM.

All publications, patents and patent applications cited in this specification are incorporated herein by reference in their entireties as if each individual publication, patent or patent application were specifically and individually indicated to be incorporated by reference. While the foregoing has been described in terms of various embodiments, the skilled artisan will appreciate that various modifications, substitutions, omissions, and changes may be made without departing from the spirit thereof. 

1-24. (canceled)
 25. An antibody that binds ACPP, wherein the antibody comprises a heavy chain variable region (HVR) comprising amino acid sequence SEQ ID NO: 83, 87, 89, or 85 and a light chain variable region (LVR) comprising amino acid sequence SEQ ID NO: 82, 86, 88, or
 84. 26. The antibody or antibody fragment of claim 25, wherein the LVR comprises the amino acid sequence SEQ ID NO: 82, and the HVR comprises the amino acid sequence SEQ ID NO:
 83. 27. The antibody or antibody fragment of claim 25, wherein the LVR comprises the amino acid sequence SEQ ID NO: 86, and the HVR comprises the amino acid sequence SEQ ID NO:
 87. 28. The antibody or antibody fragment of claim 25, wherein the LVR comprises the amino acid sequence SEQ ID NO: 88, and the HVR comprises the amino acid sequence SEQ ID NO:
 89. 29. The antibody or antibody fragment of claim 25, wherein the LVR comprises the amino acid sequence SEQ ID NO: 84, and the HVR comprises the amino acid sequence SEQ ID NO:
 85. 30. The antibody or antibody fragment of claim 25, wherein the HVR is joined to a human IgG chain constant region, and the human IgG is IgG1 or IgG3.
 31. The antibody or antibody fragment of claim 25, wherein the antibody or antibody fragment is conjugated to a cytotoxic agent, and the cytotoxic agent is a radioactive isotope or a toxin.
 32. The antibody or antibody fragment of claim 25, wherein the antibody comprises a scFv, and the LVR is connected to HVR via a linker.
 33. The antibody or antibody fragment of claim 32, wherein the scFv comprises amino acid sequence SEQ ID NO:
 173. 34. The antibody or antibody fragment of claim 32, wherein the scFv comprises amino acid sequences SEQ ID NOs: 82 and 83 that are joined by a linker.
 35. A chimeric antigen receptor (CAR) comprising an antigen binding domain comprising the antibody or fragment of claim 33, wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, the extracellular domain comprising the antigen binding domain.
 36. A chimeric antigen receptor (CAR) comprising an antigen binding domain comprising the antibody or fragment of claim 34, wherein the CAR comprises an extracellular domain, a transmembrane domain, and an intracellular domain, the extracellular domain comprising the antigen binding domain.
 37. The CAR of claim 35, wherein the intracellular domain comprises a co-stimulatory signaling region that comprises an intracellular domain of a co-stimulatory molecule, and wherein the co-stimulatory molecule comprises CD27, CD28, 4-1 BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, or a combination thereof.
 38. A modified cell comprising the CAR of claim
 35. 39. The modified cell of claim 38, wherein the modified cell is a T cell.
 40. A polynucleotide that encodes the antibody or antibody fragment of claim
 33. 41. A modified cell comprising the polynucleotide of claim
 40. 42. The modified cell of claim 41, wherein the modified cell is a T cell. 